Organic electroluminescent materials and devices

ABSTRACT

A compound that includes a ligand L, having the formula, 
     
       
         
         
             
             
         
       
     
     is provided. In the structure of Formula I, each R 1 , R 2 , R 3 , R 4 , R 4 , R 5 , R 6 , R 7 , and R 8  is independently selected from a variety of substituents; any adjacent substituents are optionally joined or fused into a ring; at least one of R 3 , R 4 , and R 5  is not hydrogen; “a” is an integer from 0 to 10; (i) when a is 0, at least one of R 7 , R 8 , and an R 2  adjacent to ring B, is not hydrogen, and (ii) when a is 1 to 10, at least one of an R 2  adjacent to ring A and an R 6  adjacent to ring C is not hydrogen; ligand L is coordinated to a metal M having an atomic weight greater than 40; and ligand L is optionally linked with other ligands to comprise a tridentate, tetradentate, pentadentate or hexadentate ligand.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a non-provisional of U.S. Patent Application Ser. No. 62/320,915, filed Apr. 11, 2016, and a non-provisional of U.S. Patent Application Ser. No. 62/368,518, filed Jul. 29, 2016, the entire contents of which are incorporated herein by reference.

FIELD

The present invention relates to compounds for use as emitters, and devices, such as organic light emitting diodes, including the same.

BACKGROUND

Opto-electronic devices that make use of organic materials are becoming increasingly desirable for a number of reasons. Many of the materials used to make such devices are relatively inexpensive, so organic opto-electronic devices have the potential for cost advantages over inorganic devices. In addition, the inherent properties of organic materials, such as their flexibility, may make them well suited for particular applications such as fabrication on a flexible substrate. Examples of organic opto-electronic devices include organic light emitting diodes/devices (OLEDs), organic phototransistors, organic photovoltaic cells, and organic photodetectors. For OLEDs, the organic materials may have performance advantages over conventional materials. For example, the wavelength at which an organic emissive layer emits light may generally be readily tuned with appropriate dopants.

OLEDs make use of thin organic films that emit light when voltage is applied across the device. OLEDs are becoming an increasingly interesting technology for use in applications such as flat panel displays, illumination, and backlighting. Several OLED materials and configurations are described in U.S. Pat. Nos. 5,844,363, 6,303,238, and 5,707,745, which are incorporated herein by reference in their entirety.

One application for phosphorescent emissive molecules is a full color display. Industry standards for such a display call for pixels adapted to emit particular colors, referred to as “saturated” colors. In particular, these standards call for saturated red, green, and blue pixels. Alternatively the OLED can be designed to emit white light. In conventional liquid crystal displays emission from a white backlight is filtered using absorption filters to produce red, green and blue emission. The same technique can also be used with OLEDs. The white OLED can be either a single EML device or a stack structure. Color may be measured using CIE coordinates, which are well known to the art.

One example of a green emissive molecule is tris(2-phenylpyridine) iridium, denoted Ir(ppy)₃, which has the following structure:

In this, and later figures herein, we depict the dative bond from nitrogen to metal (here, Ir) as a straight line.

As used herein, the term “organic” includes polymeric materials as well as small molecule organic materials that may be used to fabricate organic opto-electronic devices. “Small molecule” refers to any organic material that is not a polymer, and “small molecules” may actually be quite large. Small molecules may include repeat units in some circumstances. For example, using a long chain alkyl group as a substituent does not remove a molecule from the “small molecule” class. Small molecules may also be incorporated into polymers, for example as a pendent group on a polymer backbone or as a part of the backbone. Small molecules may also serve as the core moiety of a dendrimer, which consists of a series of chemical shells built on the core moiety. The core moiety of a dendrimer may be a fluorescent or phosphorescent small molecule emitter. A dendrimer may be a “small molecule,” and it is believed that all dendrimers currently used in the field of OLEDs are small molecules.

As used herein, “top” means furthest away from the substrate, while “bottom” means closest to the substrate. Where a first layer is described as “disposed over” a second layer, the first layer is disposed further away from substrate. There may be other layers between the first and second layer, unless it is specified that the first layer is “in contact with” the second layer. For example, a cathode may be described as “disposed over” an anode, even though there are various organic layers in between.

As used herein, “solution processible” means capable of being dissolved, dispersed, or transported in and/or deposited from a liquid medium, either in solution or suspension form.

A ligand may be referred to as “photoactive” when it is believed that the ligand directly contributes to the photoactive properties of an emissive material. A ligand may be referred to as “ancillary” when it is believed that the ligand does not contribute to the photoactive properties of an emissive material, although an ancillary ligand may alter the properties of a photoactive ligand.

As used herein, and as would be generally understood by one skilled in the art, a first “Highest Occupied Molecular Orbital” (HOMO) or “Lowest Unoccupied Molecular Orbital” (LUMO) energy level is “greater than” or “higher than” a second HOMO or LUMO energy level if the first energy level is closer to the vacuum energy level. Since ionization potentials (IP) are measured as a negative energy relative to a vacuum level, a higher HOMO energy level corresponds to an IP having a smaller absolute value (an IP that is less negative). Similarly, a higher LUMO energy level corresponds to an electron affinity (EA) having a smaller absolute value (an EA that is less negative). On a conventional energy level diagram, with the vacuum level at the top, the LUMO energy level of a material is higher than the HOMO energy level of the same material. A “higher” HOMO or LUMO energy level appears closer to the top of such a diagram than a “lower” HOMO or LUMO energy level.

As used herein, and as would be generally understood by one skilled in the art, a first work function is “greater than” or “higher than” a second work function if the first work function has a higher absolute value. Because work functions are generally measured as negative numbers relative to vacuum level, this means that a “higher” work function is more negative. On a conventional energy level diagram, with the vacuum level at the top, a “higher” work function is illustrated as further away from the vacuum level in the downward direction. Thus, the definitions of HOMO and LUMO energy levels follow a different convention than work functions.

More details on OLEDs, and the definitions described above, can be found in U.S. Pat. No. 7,279,704, which is incorporated herein by reference in its entirety.

SUMMARY

According to an embodiment, a compound is provided that includes a ligand L, having the formula,

In the structure of Formula I:

R¹ and R⁶ represent mono, di, tri, or tetra substitution, or no substitution;

R² represents mono, di, or tri substitution, or no substitution;

each R¹, R², R³, R⁴, R⁴, R⁵, R⁶, R⁷, and R⁸ is independently selected from the group consisting of hydrogen, deuterium, halide, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acids, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof;

any adjacent substituents of R¹ R², R³, R⁴, R⁵, R⁶, R⁷, and R⁸ are optionally joined or fused into a ring;

at least one of R³, R⁴, and R⁵ is not hydrogen;

a is an integer from 0 to 10;

(i) when a is 0, at least one of R⁷, R⁸, and an R² adjacent to ring B, is not hydrogen, and (ii) when a is 1 to 10, at least one of an R² adjacent to ring A and an R⁶ adjacent to ring C is not hydrogen;

the ligand L is coordinated to a metal M having an atomic weight greater than 40; and

the ligand L is optionally linked with other ligands to comprise a tridentate, tetradentate, pentadentate or hexadentate ligand.

According to another embodiment, an organic light emitting diode/device (OLED) is also provided. The OLED can include an anode, a cathode, and an organic layer, disposed between the anode and the cathode. The organic layer can include a compound that includes a ligand L, having the formula,

According to yet another embodiment, the organic light emitting device is incorporated into one or more device selected from a consumer product, an electronic component module, and/or a lighting panel.

According to yet another embodiment, a formulation containing a compound including a ligand L, having the formula,

is provided.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows an organic light emitting device.

FIG. 2 shows an inverted organic light emitting device that does not have a separate electron transport layer.

DETAILED DESCRIPTION

Generally, an OLED comprises at least one organic layer disposed between and electrically connected to an anode and a cathode. When a current is applied, the anode injects holes and the cathode injects electrons into the organic layer(s). The injected holes and electrons each migrate toward the oppositely charged electrode. When an electron and hole localize on the same molecule, an “exciton,” which is a localized electron-hole pair having an excited energy state, is formed. Light is emitted when the exciton relaxes via a photoemissive mechanism. In some cases, the exciton may be localized on an excimer or an exciplex. Non-radiative mechanisms, such as thermal relaxation, may also occur, but are generally considered undesirable.

The initial OLEDs used emissive molecules that emitted light from their singlet states (“fluorescence”) as disclosed, for example, in U.S. Pat. No. 4,769,292, which is incorporated by reference in its entirety. Fluorescent emission generally occurs in a time frame of less than 10 nanoseconds.

More recently, OLEDs having emissive materials that emit light from triplet states (“phosphorescence”) have been demonstrated. Baldo et al., “Highly Efficient Phosphorescent Emission from Organic Electroluminescent Devices,” Nature, vol. 395, 151-154, 1998; (“Baldo-I”) and Baldo et al., “Very high-efficiency green organic light-emitting devices based on electrophosphorescence,” Appl. Phys. Lett., vol. 75, No. 3, 4-6 (1999) (“Baldo-II”), are incorporated by reference in their entireties. Phosphorescence is described in more detail in U.S. Pat. No. 7,279,704 at cols. 5-6, which are incorporated by reference.

FIG. 1 shows an organic light emitting device 100. The figures are not necessarily drawn to scale. Device 100 may include a substrate 110, an anode 115, a hole injection layer 120, a hole transport layer 125, an electron blocking layer 130, an emissive layer 135, a hole blocking layer 140, an electron transport layer 145, an electron injection layer 150, a protective layer 155, a cathode 160, and a barrier layer 170. Cathode 160 is a compound cathode having a first conductive layer 162 and a second conductive layer 164. Device 100 may be fabricated by depositing the layers described, in order. The properties and functions of these various layers, as well as example materials, are described in more detail in U.S. Pat. No. 7,279,704 at cols. 6-10, which are incorporated by reference.

More examples for each of these layers are available. For example, a flexible and transparent substrate-anode combination is disclosed in U.S. Pat. No. 5,844,363, which is incorporated by reference in its entirety. An example of a p-doped hole transport layer is m-MTDATA doped with F₄-TCNQ at a molar ratio of 50:1, as disclosed in U.S. Patent Application Publication No. 2003/0230980, which is incorporated by reference in its entirety. Examples of emissive and host materials are disclosed in U.S. Pat. No. 6,303,238 to Thompson et al., which is incorporated by reference in its entirety. An example of an n-doped electron transport layer is BPhen doped with Li at a molar ratio of 1:1, as disclosed in U.S. Patent Application Publication No. 2003/0230980, which is incorporated by reference in its entirety. U.S. Pat. Nos. 5,703,436 and 5,707,745, which are incorporated by reference in their entireties, disclose examples of cathodes including compound cathodes having a thin layer of metal such as Mg:Ag with an overlying transparent, electrically-conductive, sputter-deposited ITO layer. The theory and use of blocking layers is described in more detail in U.S. Pat. No. 6,097,147 and U.S. Patent Application Publication No. 2003/0230980, which are incorporated by reference in their entireties. Examples of injection layers are provided in U.S. Patent Application Publication No. 2004/0174116, which is incorporated by reference in its entirety. A description of protective layers may be found in U.S. Patent Application Publication No. 2004/0174116, which is incorporated by reference in its entirety.

FIG. 2 shows an inverted OLED 200. The device includes a substrate 210, a cathode 215, an emissive layer 220, a hole transport layer 225, and an anode 230. Device 200 may be fabricated by depositing the layers described, in order. Because the most common OLED configuration has a cathode disposed over the anode, and device 200 has cathode 215 disposed under anode 230, device 200 may be referred to as an “inverted” OLED. Materials similar to those described with respect to device 100 may be used in the corresponding layers of device 200. FIG. 2 provides one example of how some layers may be omitted from the structure of device 100.

The simple layered structure illustrated in FIGS. 1 and 2 is provided by way of non-limiting example, and it is understood that embodiments of the invention may be used in connection with a wide variety of other structures. The specific materials and structures described are exemplary in nature, and other materials and structures may be used. Functional OLEDs may be achieved by combining the various layers described in different ways, or layers may be omitted entirely, based on design, performance, and cost factors. Other layers not specifically described may also be included. Materials other than those specifically described may be used. Although many of the examples provided herein describe various layers as comprising a single material, it is understood that combinations of materials, such as a mixture of host and dopant, or more generally a mixture, may be used. Also, the layers may have various sublayers. The names given to the various layers herein are not intended to be strictly limiting. For example, in device 200, hole transport layer 225 transports holes and injects holes into emissive layer 220, and may be described as a hole transport layer or a hole injection layer. In one embodiment, an OLED may be described as having an “organic layer” disposed between a cathode and an anode. This organic layer may comprise a single layer, or may further comprise multiple layers of different organic materials as described, for example, with respect to FIGS. 1 and 2.

Structures and materials not specifically described may also be used, such as OLEDs comprised of polymeric materials (PLEDs) such as disclosed in U.S. Pat. No. 5,247,190 to Friend et al., which is incorporated by reference in its entirety. By way of further example, OLEDs having a single organic layer may be used. OLEDs may be stacked, for example as described in U.S. Pat. No. 5,707,745 to Forrest et al, which is incorporated by reference in its entirety. The OLED structure may deviate from the simple layered structure illustrated in FIGS. 1 and 2. For example, the substrate may include an angled reflective surface to improve out-coupling, such as a mesa structure as described in U.S. Pat. No. 6,091,195 to Forrest et al., and/or a pit structure as described in U.S. Pat. No. 5,834,893 to Bulovic et al., which are incorporated by reference in their entireties.

Unless otherwise specified, any of the layers of the various embodiments may be deposited by any suitable method. For the organic layers, preferred methods include thermal evaporation, ink-jet, such as described in U.S. Pat. Nos. 6,013,982 and 6,087,196, which are incorporated by reference in their entireties, organic vapor phase deposition (OVPD), such as described in U.S. Pat. No. 6,337,102 to Forrest et al., which is incorporated by reference in its entirety, and deposition by organic vapor jet printing (OVJP), such as described in U.S. Pat. No. 7,431,968, which is incorporated by reference in its entirety. Other suitable deposition methods include spin coating and other solution based processes. Solution based processes are preferably carried out in nitrogen or an inert atmosphere. For the other layers, preferred methods include thermal evaporation. Preferred patterning methods include deposition through a mask, cold welding such as described in U.S. Pat. Nos. 6,294,398 and 6,468,819, which are incorporated by reference in their entireties, and patterning associated with some of the deposition methods such as ink-jet and OVJD. Other methods may also be used. The materials to be deposited may be modified to make them compatible with a particular deposition method. For example, substituents such as alkyl and aryl groups, branched or unbranched, and preferably containing at least 3 carbons, may be used in small molecules to enhance their ability to undergo solution processing. Substituents having 20 carbons or more may be used, and 3-20 carbons is a preferred range. Materials with asymmetric structures may have better solution processability than those having symmetric structures, because asymmetric materials may have a lower tendency to recrystallize. Dendrimer substituents may be used to enhance the ability of small molecules to undergo solution processing.

Devices fabricated in accordance with embodiments of the present invention may further optionally comprise a barrier layer. One purpose of the barrier layer is to protect the electrodes and organic layers from damaging exposure to harmful species in the environment including moisture, vapor and/or gases, etc. The barrier layer may be deposited over, under or next to a substrate, an electrode, or over any other parts of a device including an edge. The barrier layer may comprise a single layer, or multiple layers. The barrier layer may be formed by various known chemical vapor deposition techniques and may include compositions having a single phase as well as compositions having multiple phases. Any suitable material or combination of materials may be used for the barrier layer. The barrier layer may incorporate an inorganic or an organic compound or both. The preferred barrier layer comprises a mixture of a polymeric material and a non-polymeric material as described in U.S. Pat. No. 7,968,146, PCT Pat. Application Nos. PCT/US2007/023098 and PCT/US2009/042829, which are herein incorporated by reference in their entireties. To be considered a “mixture”, the aforesaid polymeric and non-polymeric materials comprising the barrier layer should be deposited under the same reaction conditions and/or at the same time. The weight ratio of polymeric to non-polymeric material may be in the range of 95:5 to 5:95. The polymeric material and the non-polymeric material may be created from the same precursor material. In one example, the mixture of a polymeric material and a non-polymeric material consists essentially of polymeric silicon and inorganic silicon.

Devices fabricated in accordance with embodiments of the invention can be incorporated into a wide variety of electronic component modules (or units) that can be incorporated into a variety of electronic products or intermediate components. Examples of such electronic products or intermediate components include display screens, lighting devices such as discrete light source devices or lighting panels, etc. that can be utilized by the end-user product manufacturers. Such electronic component modules can optionally include the driving electronics and/or power source(s). Devices fabricated in accordance with embodiments of the invention can be incorporated into a wide variety of consumer products that have one or more of the electronic component modules (or units) incorporated therein. Such consumer products would include any kind of products that include one or more light source(s) and/or one or more of some type of visual displays. Some examples of such consumer products include flat panel displays, computer monitors, medical monitors, televisions, billboards, lights for interior or exterior illumination and/or signaling, heads-up displays, fully or partially transparent displays, flexible displays, laser printers, telephones, mobile phones, tablets, phablets, personal digital assistants (PDAs), wearable devices, laptop computers, digital cameras, camcorders, viewfinders, micro-displays (displays that are less than 2 inches diagonal), 3-D displays, virtual reality or augmented reality displays, vehicles, video walls comprising multiple displays tiled together, theater or stadium screen, and a sign. Various control mechanisms may be used to control devices fabricated in accordance with the present invention, including passive matrix and active matrix. Many of the devices are intended for use in a temperature range comfortable to humans, such as 18 degrees C. to 30 degrees C., and more preferably at room temperature (20-25 degrees C.), but could be used outside this temperature range, for example, from −40 degree C. to +80 degree C.

The materials and structures described herein may have applications in devices other than OLEDs. For example, other optoelectronic devices such as organic solar cells and organic photodetectors may employ the materials and structures. More generally, organic devices, such as organic transistors, may employ the materials and structures.

The term “halo,” “halogen,” or “halide” as used herein includes fluorine, chlorine, bromine, and iodine.

The term “alkyl” as used herein contemplates both straight and branched chain alkyl radicals. Preferred alkyl groups are those containing from one to fifteen carbon atoms and includes methyl, ethyl, propyl, 1-methylethyl, butyl, 1-methylpropyl, 2-methylpropyl, pentyl, 1-methylbutyl, 2-methylbutyl, 3-methylbutyl, 1,1-dimethylpropyl, 1,2-dimethylpropyl, 2,2-dimethylpropyl, and the like. Additionally, the alkyl group may be optionally substituted.

The term “cycloalkyl” as used herein contemplates cyclic alkyl radicals. Preferred cycloalkyl groups are those containing 3 to 10 ring carbon atoms and includes cyclopropyl, cyclopentyl, cyclohexyl, adamantyl, and the like. Additionally, the cycloalkyl group may be optionally substituted.

The term “alkenyl” as used herein contemplates both straight and branched chain alkene radicals. Preferred alkenyl groups are those containing two to fifteen carbon atoms. Additionally, the alkenyl group may be optionally substituted.

The term “alkynyl” as used herein contemplates both straight and branched chain alkyne radicals. Preferred alkynyl groups are those containing two to fifteen carbon atoms. Additionally, the alkynyl group may be optionally substituted.

The terms “aralkyl” or “arylalkyl” as used herein are used interchangeably and contemplate an alkyl group that has as a substituent an aromatic group. Additionally, the aralkyl group may be optionally substituted.

The term “heterocyclic group” as used herein contemplates aromatic and non-aromatic cyclic radicals. Hetero-aromatic cyclic radicals also means heteroaryl. Preferred hetero-non-aromatic cyclic groups are those containing 3 to 7 ring atoms which includes at least one hetero atom, and includes cyclic amines such as morpholino, piperidino, pyrrolidino, and the like, and cyclic ethers, such as tetrahydrofuran, tetrahydropyran, and the like. Additionally, the heterocyclic group may be optionally substituted.

The term “aryl” or “aromatic group” as used herein contemplates single-ring groups and polycyclic ring systems. The polycyclic rings may have two or more rings in which two carbons are common to two adjoining rings (the rings are “fused”) wherein at least one of the rings is aromatic, e.g., the other rings can be cycloalkyls, cycloalkenyls, aryl, heterocycles, and/or heteroaryls. Preferred aryl groups are those containing six to thirty carbon atoms, preferably six to twenty carbon atoms, more preferably six to twelve carbon atoms. Especially preferred is an aryl group having six carbons, ten carbons or twelve carbons. Suitable aryl groups include phenyl, biphenyl, triphenyl, triphenylene, tetraphenylene, naphthalene, anthracene, phenalene, phenanthrene, fluorene, pyrene, chrysene, perylene, and azulene, preferably phenyl, biphenyl, triphenyl, triphenylene, fluorene, and naphthalene. Additionally, the aryl group may be optionally substituted.

The term “heteroaryl” as used herein contemplates single-ring hetero-aromatic groups that may include from one to five heteroatoms. The term heteroaryl also includes polycyclic hetero-aromatic systems having two or more rings in which two atoms are common to two adjoining rings (the rings are “fused”) wherein at least one of the rings is a heteroaryl, e.g., the other rings can be cycloalkyls, cycloalkenyls, aryl, heterocycles, and/or heteroaryls. Preferred heteroaryl groups are those containing three to thirty carbon atoms, preferably three to twenty carbon atoms, more preferably three to twelve carbon atoms. Suitable heteroaryl groups include dibenzothiophene, dibenzofuran, dibenzoselenophene, furan, thiophene, benzofuran, benzothiophene, benzoselenophene, carbazole, indolocarbazole, pyridylindole, pyrrolodipyridine, pyrazole, imidazole, triazole, oxazole, thiazole, oxadiazole, oxatriazole, dioxazole, thiadiazole, pyridine, pyridazine, pyrimidine, pyrazine, triazine, oxazine, oxathiazine, oxadiazine, indole, benzimidazole, indazole, indoxazine, benzoxazole, benzisoxazole, benzothiazole, quinoline, isoquinoline, cinnoline, quinazoline, quinoxaline, naphthyridine, phthalazine, pteridine, xanthene, acridine, phenazine, phenothiazine, phenoxazine, benzofuropyridine, furodipyridine, benzothienopyridine, thienodipyridine, benzoselenophenopyridine, and selenophenodipyridine, preferably dibenzothiophene, dibenzofuran, dibenzoselenophene, carbazole, indolocarbazole, imidazole, pyridine, triazine, benzimidazole, 1,2-azaborine, 1,3-azaborine, 1,4-azaborine, borazine, and aza-analogs thereof. Additionally, the heteroaryl group may be optionally substituted.

The alkyl, cycloalkyl, alkenyl, alkynyl, aralkyl, heterocyclic group, aryl, and heteroaryl may be unsubstituted or may be substituted with one or more substituents selected from the group consisting of deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, cyclic amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acid, ether, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof.

As used herein, “substituted” indicates that a substituent other than H is bonded to the relevant position, such as carbon. Thus, for example, where R¹ is mono-substituted, then one R¹ must be other than H. Similarly, where R¹ is di-substituted, then two of R¹ must be other than H. Similarly, where R¹ is unsubstituted, R¹ is hydrogen for all available positions.

The “aza” designation in the fragments described herein, i.e. aza-dibenzofuran, aza-dibenzothiophene, etc. means that one or more of the C—H groups in the respective fragment can be replaced by a nitrogen atom, for example, and without any limitation, azatriphenylene encompasses both dibenzo[f,h]quinoxaline and dibenzo[f,h]quinoline. One of ordinary skill in the art can readily envision other nitrogen analogs of the aza-derivatives described above, and all such analogs are intended to be encompassed by the terms as set forth herein.

It is to be understood that when a molecular fragment is described as being a substituent or otherwise attached to another moiety, its name may be written as if it were a fragment (e.g. phenyl, phenylene, naphthyl, dibenzofuryl) or as if it were the whole molecule (e.g. benzene, naphthalene, dibenzofuran). As used herein, these different ways of designating a substituent or attached fragment are considered to be equivalent.

According to one embodiment, a compound comprising a ligand L, having the formula,

is described. In the structure of Formula I:

R¹ and R⁶ represent mono, di, tri, or tetra substitution, or no substitution;

R² represents mono, di, or tri substitution, or no substitution;

-   -   each R¹, R², R³, R⁴, R⁴, R⁵, R⁶, R⁷, and R⁸ is independently         selected from the group consisting of hydrogen, deuterium,         halide, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy,         aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl,         alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acids,         ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl,         phosphino, and combinations thereof;

any adjacent substituents of R′ R², R³, R⁴, R⁵, R⁶, R⁷, and R⁸ are optionally joined or fused into a ring;

at least one of R³, R⁴, and R⁵ is not hydrogen;

a is an integer from 0 to 10;

(i) when a is 0, at least one of R⁷, R⁸, and an R² adjacent to ring B, is not hydrogen, and (ii) when a is 1 to 10, at least one of an R² adjacent to ring A and an R⁶ adjacent to ring C is not hydrogen;

the ligand L is coordinated to a metal M having an atomic weight greater than 40; and

the ligand L is optionally linked with other ligands to comprise a tridentate, tetradentate, pentadentate or hexadentate ligand.

In some embodiments, ring A is bonded to ring C at a position para to the N of ring C. In some embodiments, ring A is bonded to ring C as a position meta to the N of ring C. In some embodiments, ring B is bonded to ring C at a position para to the N of ring C or ring B is bonded to the adjacent ring A at a position para to ring C or an adjacent ring A. In some embodiments, ring B is bonded to ring C at a position meta to the N of ring C or ring B is bonded to the adjacent ring A at a position meta to ring C or an adjacent ring A.

In some embodiments, M is selected from the group consisting of Ir, Rh, Re, Ru, Os, Pt, Au, and Cu. In some embodiments, M is Ir or Pt.

In some embodiments, the compound is homoleptic. In other embodiments, the compound is heteroleptic.

In some embodiments, (i) when a is 0, at least one of R⁷, R⁸, and an R² adjacent to ring B, is selected from the group consisting of alkyl, cycloalkyl, partially or fully deuterated variants thereof, and combinations thereof, and (ii) when a is 1 to 10, at least one R² adjacent to ring A and an R⁶ adjacent to ring C is selected from the group consisting of alkyl, cycloalkyl, partially or fully deuterated variants thereof, and combinations thereof.

In some embodiments, at least one of R³, R⁴, and R⁵ is selected from the group consisting of alkyl, cycloalkyl, fluorine, partially or fully deuterated variants thereof, and combinations thereof.

In some embodiments, R¹ is hydrogen.

In some embodiments, (i) when a is 0, at least one R² adjacent to ring B is not hydrogen, and at least one of R⁷ and R⁸ is not hydrogen, and (ii) when a is 1 to 10, at least at one R² adjacent to ring A is not hydrogen, and at least one R⁶ adjacent to ring C is not hydrogen.

In some embodiments, when a is 1 to 10, R⁷ and R⁸ are hydrogen. In some embodiments, a is 2 to 10.

In some embodiments, ligand L is selected from the group consisting of:

In some embodiments, ligand L is selected from the group consisting of L^(A1) to L^(A1432), L^(B1) to L^(B1432), L^(C1) to L^(C1432), L^(D1) to L^(D1432) as defined in the following table based on the structures of

i in L^(Ai), L^(Bi), L^(Ci), L^(Di) R² R³ R⁴ R⁵ R⁷ or R⁶¹ R⁸ or R⁶² 1. CH₃ H CH₃ H H CH₃ 2. CH₃ H CH₂CH₃ H H CH₃ 3. CH₃ H CH(CH₃)₂ H H CH₃ 4. CH₃ H CH₂CH(CH₃)₂ H H CH₃ 5. CH₃ H C(CH₃)₃ H H CH₃ 6. CH₃ H CH₂C(CH₃)₃ H H CH₃ 7. CH₃ H CH₂CH₂CF₃ H H CH₃ 8. CH₃ H CH₂CCF₃(CH₃)₂ H H CH₃ 9. CH₃ H

H H CH₃ 10. CH₃ H

H H CH₃ 11. CH₃ H

H H CH₃ 12. CH₃ H

H H CH₃ 13. CH₃ H

H H CH₃ 14. CH₃ H

H H CH₃ 15. CH₃ H

H H CH₃ 16. CH₃ H

H H CH₃ 17. CH₃ H

H H CH₃ 18. CH₃ H

H H CH₃ 19. CH₃ H

H H CH₃ 20. CH₃ H

H H CH₃ 21. CH₃ H

H H CH₃ 22. CH₃ H

H H CH₃ 23. CH₃ H

H H CH₃ 24. CH₃ H

H H CH₃ 25. CH₃ H

H H CH₃ 26. CH₃ H

H H CH₃ 27. CH₃ H CH₃ H CH₃ CH₃ 28. CH₃ H CH₂CH₃ H CH₃ CH₃ 29. CH₃ H CH(CH₃)₂ H CH₃ CH₃ 30. CH₃ H CH₂CH(CH₃)₂ H CH₃ CH₃ 31. CH₃ H C(CH₃)₃ H CH₃ CH₃ 32. CH₃ H CH₂C(CH₃)₃ H CH₃ CH₃ 33. CH₃ H CH₂CH₂CF₃ H CH₃ CH₃ 34. CH₃ H CH₂CCF₃(CH₃)₂ H CH₃ CH₃ 35. CH₃ H

H CH₃ CH₃ 36. CH₃ H

H CH₃ CH₃ 37. CH₃ H

H CH₃ CH₃ 38. CH₃ H

H CH₃ CH₃ 39. CH₃ H

H CH₃ CH₃ 40. CH₃ H

H CH₃ CH₃ 41. CH₃ H

H CH₃ CH₃ 42. CH₃ H

H CH₃ CH₃ 43. CH₃ H

H CH₃ CH₃ 44. CH₃ H

H CH₃ CH₃ 45. CH₃ H

H CH₃ CH₃ 46. CH₃ H

H CH₃ CH₃ 47. CH₃ H

H CH₃ CH₃ 48. CH₃ H

H CH₃ CH₃ 49. CH₃ H

H CH₃ CH₃ 50. CH₃ H

H CH₃ CH₃ 51. CH₃ H

H CH₃ CH₃ 52. CH₃ H

H CH₃ CH₃ 53. H H CH₃ H H CH₃ 54. H H CH₂CH₃ H H CH₃ 55. CH(CH₃)₂ H H CH₃ 56. H H CH₂CH(CH₃)₂ H H CH₃ 57. H H C(CH₃)₃ H H CH₃ 58. H H CH₂C(CH₃)₃ H H CH₃ 59. H H CH₂CH₂CF₃ H H CH₃ 60. H H CH₂CCF₃(CH₃)₂ H H CH₃ 61. H H

H H CH₃ 62. H H

H H CH₃ 63. H H

H H CH₃ 64. H H

H H CH₃ 65. H H

H H CH₃ 66. H H

H H CH₃ 67. H H

H H CH₃ 68. H H

H H CH₃ 69. H H

H H CH₃ 70. H H

H H CH₃ 71. H H

H H CH₃ 72. H H

H H CH₃ 73. H H

H H CH₃ 74. H H

H H CH₃ 75. H H

H H CH₃ 76. H H

H H CH₃ 77. H H

H H CH₃ 78. H H

H H CH₃ 79. H H CH₃ H CH₃ CH₃ 80. H H CH₂CH₃ H CH₃ CH₃ 81. H H CH(CH₃)₂ H CH₃ CH₃ 82. H H CH₂CH(CH₃)₂ H CH₃ CH₃ 83. H H C(CH₃)₃ H CH₃ CH₃ 84. H H CH₂C(CH₃)₃ H CH₃ CH₃ 85. H H CH₂CH₂CF₃ H CH₃ CH₃ 86. H H CH₂CCF₃(CH₃)₂ H CH₃ CH₃ 87. H H

H CH₃ CH₃ 88. H H

H CH₃ CH₃ 89. H H

H CH₃ CH₃ 90. H H

H CH₃ CH₃ 91. H H

H CH₃ CH₃ 92. H H

H CH₃ CH₃ 93. H H

H CH₃ CH₃ 94. H H

H CH₃ CH₃ 95. H H

H CH₃ CH₃ 96. H H

H CH₃ CH₃ 97. H H

H CH₃ CH₃ 98. H H

H CH₃ CH₃ 99. H H

H CH₃ CH₃ 100. H H

H CH₃ CH₃ 101. H H

H CH₃ CH₃ 102. H H

H CH₃ CH₃ 103. H H

H CH₃ CH₃ 104. H H

H CH₃ CH₃ 105. CH₃ H CH₃ CH₃ H CH₃ 106. CH₃ H CH₂CH₃ CH₃ H CH₃ 107. CH₃ H CH(CH₃)₂ CH₃ H CH₃ 108. CH₃ H CH₂CH(CH₃)₂ CH₃ H CH₃ 109. CH₃ H C(CH₃)₃ CH₃ H CH₃ 110. CH₃ H CH₂C(CH₃)₃ CH₃ H CH₃ 111. CH₃ H CH₂CH₂CF₃ CH₃ H CH₃ 112. CH₃ H CH₂CCF₃(CH₃)₂ CH₃ H CH₃ 113. CH₃ H

CH₃ H CH₃ 114. CH₃ H

CH₃ H CH₃ 115. CH₃ H

CH₃ H CH₃ 116. CH₃ H

CH₃ H CH₃ 117. CH₃ H

CH₃ H CH₃ 118. CH₃ H

CH₃ H CH₃ 119. CH₃ H

CH₃ H CH₃ 120. CH₃ H

CH₃ H CH₃ 121. CH₃ H

CH₃ H CH₃ 122. CH₃ H

CH₃ H CH₃ 123. CH₃ H

CH₃ H CH₃ 124. CH₃ H

CH₃ H CH₃ 125. CH₃ H

CH₃ H CH₃ 126. CH₃ H

CH₃ H CH₃ 127. CH₃ H

CH₃ H CH₃ 128. CH₃ H

CH₃ H CH₃ 129. CH₃ H

CH₃ H CH₃ 130. CH₃ H

CH₃ H CH₃ 131. CH₃ CH₃ CH₃ CH₃ H CH₃ 132. CH₃ CH₃ CH₂CH₃ CH₃ H CH₃ 133. CH₃ CH₃ CH(CH₃)₂ CH₃ H CH₃ 134. CH₃ CH₃ CH₂CH(CH₃)₂ CH₃ H CH₃ 135. CH₃ CH₃ C(CH₃)₃ CH₃ H CH₃ 136. CH₃ CH₃ CH₂C(CH₃)₃ CH₃ H CH₃ 137. CH₃ CH₃ CH₂CH₂CF₃ CH₃ H CH₃ 138. CH₃ CH₃ CH₂CCF₃(CH₃)₂ CH₃ H CH₃ 139. CH₃ CH₃

CH₃ H CH₃ 140. CH₃ CH₃

CH₃ H CH₃ 141. CH₃ CH₃

CH₃ H CH₃ 142. CH₃ CH₃

CH₃ H CH₃ 143. CH₃ CH₃

CH₃ H CH₃ 144. CH₃ CH₃

CH₃ H CH₃ 145. CH₃ CH₃

CH₃ H CH₃ 146. CH₃ CH₃

CH₃ H CH₃ 147. CH₃ CH₃

CH₃ H CH₃ 148. CH₃ CH₃

CH₃ H CH₃ 149. CH₃ CH₃

CH₃ H CH₃ 150. CH₃ CH₃

CH₃ H CH₃ 151. CH₃ CH₃

CH₃ H CH₃ 152. CH₃ CH₃

CH₃ H CH₃ 153. CH₃ CH₃

CH₃ H CH₃ 154. CH₃ CH₃

CH₃ H CH₃ 155. CH₃ CH₃

CH₃ H CH₃ 156. CH₃ CH₃

CH₃ H CH₃ 157. CH₃ CH₃

CH₃ H CH₃ 158. CH₃ CH₃

CH₃ H CH₃ 159. CD₃ H CD₃ H H CD₃ 160. CD₃ H CD₃CD₃ H H CD₃ 161. CD₃ H CD₂CH₃ H H CD₃ 162. CD₃ H CD(CD₃)₂ H H CD₃ 163. CD₃ H CD(CH₃)₂ H H CD₃ 164. CD₃ H CD₂CD(CD₃)₂ H H CD₃ 165. CD₃ H CD₂CH(CH₃)₂ H H CD₃ 166. CD₃ H CD₂C(CD₃)₃ H H CD₃ 167. CD₃ H CD₂C(CH₃)₃ H H CD₃ 168. CD₃ H CD₂CD₂CF₃ H H CD₃ 169. CD₃ H CD₂CH₂CF₃ H H CD₃ 170. CD₃ H CD₂CCF₃(CH₃)₂ H H CD₃ 171. CD₃ H

H H CD₃ 172. CD₃ H

H H CD₃ 173. CD₃ H

H H CD₃ 174. CD₃ H

H H CD₃ 175. CD₃ H

H H CD₃ 176. CD₃ H

H H CD₃ 177. CD₃ H

H H CD₃ 178. CD₃ H

H H CD₃ 179. CD₃ H

H H CD₃ 180. CD₃ H

H H CD₃ 181. CD₃ H

H H CD₃ 182. CD₃ H

H H CD₃ 183. CD₃ H

H H CD₃ 184. CD₃ H

H H CD₃ 185. CD₃ H

H H CD₃ 186. CD₃ H

H H CD₃ 187. CD₃ H

H H CD₃ 188. CD₃ H

H H CD₃ 189. CD₃ H

H H CD₃ 190. CD₃ H

H H CD₃ 191. CD₃ H CD₃ H CD₃ CD₃ 192. CD₃ H CD₂CD₃ H CD₃ CD₃ 193. CD₃ H CD₂CH₃ H CD₃ CD₃ 194. CD₃ H CD(CD₃)₂ H CD₃ CD₃ 195. CD₃ H CD(CH₃)₂ H CD₃ CD₃ 196. CD₃ H CD₂CD(CD₃)₂ H CD₃ CD₃ 197. CD₃ H CD₂CH(CH₃)₂ H CD₃ CD₃ 198. CD₃ H CD₂C(CD₃)₃ H CD₃ CD₃ 199. CD₃ H CD₂C(CH₃)₃ H CD₃ CD₃ 200. CD₃ H CD₂CD₂CF₃ H CD₃ CD₃ 201. CD₃ H CD₂CH₂CF₃ H CD₃ CD₃ 202. CD₃ H CD₂CCF₃(CH₃)₂ H CD₃ CD₃ 203. CD₃ H

H CD₃ CD₃ 204. CD₃ H

H CD₃ CD₃ 205. CD₃ H

H CD₃ CD₃ 206. CD₃ H

H CD₃ CD₃ 207. CD₃ H

H CD₃ CD₃ 208. CD₃ H

H CD₃ CD₃ 209. CD₃ H

H CD₃ CD₃ 210. CD₃ H

H CD₃ CD₃ 211. CD₃ H

H CD₃ CD₃ 212. CD₃ H

H CD₃ CD₃ 213. CD₃ H

H CD₃ CD₃ 214. CD₃ H

H CD₃ CD₃ 215. CD₃ H

H CD₃ CD₃ 216. CD₃ H

H CD₃ CD₃ 217. CD₃ H

H CD₃ CD₃ 218. CD₃ H

H CD₃ CD₃ 219. CD₃ H

H CD₃ CD₃ 220. CD₃ H

H CD₃ CD₃ 221. CD₃ H

H CD₃ CD₃ 222. CD₃ H

H CD₃ CD₃ 223. H H CD₃ H H CD₃ 224. H H CD₂CD₃ H H CD₃ 225. H H CD₂CH₃ H H CD₃ 226. H H CD(CD₃)₂ H H CD₃ 227. H H CD(CH₃)₂ H H CD₃ 228. H H CD₂CD(CD₃)₂ H H CD₃ 229. H H CD₂CH(CH₃)₂ H H CD₃ 230. H H CD₂C(CD₃)₃ H H CD₃ 231. H H CD₂C(CH₃)₃ H H CD₃ 232. H H CD₂CD₂CF₃ H H CD₃ 233. H H CD₂CH₂CF₃ H H CD₃ 234. H H CD₂CCF₃(CH₃)₂ H H CD₃ 235. H H

H H CD₃ 236. H H

H H CD₃ 237. H H

H H CD₃ 238. H H

H H CD₃ 239. H H

H H CD₃ 240. H H

H H CD₃ 241. H H

H H CD₃ 242. H H

H H CD₃ 243. H H

H H CD₃ 244. H H

H H CD₃ 245. H H

H H CD₃ 246. H H

H H CD₃ 247. H H

H H CD₃ 248. H H

H H CD₃ 249. H H

H H CD₃ 250. H H

H H CD₃ 251. H H

H H CD₃ 252. H H

H H CD₃ 253. H H

H H CD₃ 254. H H

H H CD₃ 255. H H CD₃ H CD₃ CD₃ 256. H H CD₂CD₃ H CD₃ CD₃ 257. H H CD₂CH₃ H CD₃ CD₃ 258. H H CD(CD₃)₂ H CD₃ CD₃ 259. H H CD(CH₃)₂ H CD₃ CD₃ 260. H H CD₂CD(CD₃)₂ H CD₃ CD₃ 261. H H CD₂CH(CH₃)₂ H CD₃ CD₃ 262. H H CD₂C(CD₃)₃ H CD₃ CD₃ 263. H H CD₂C(CH₃)₃ H CD₃ CD₃ 264. H H CD₂CD₂CF₃ H CD₃ CD₃ 265. H H CD₂CH₂CF₃ H CD₃ CD₃ 266. H H CD₂CCF₃(CH₃)₂ H CD₃ CD₃ 267. H H

H CD₃ CD₃ 268. H H

H CD₃ CD₃ 269. H H

H CD₃ CD₃ 270. H H

H CD₃ CD₃ 271. H H

H CD₃ CD₃ 272. H H

H CD₃ CD₃ 273. H H

H CD₃ CD₃ 274. H H

H CD₃ CD₃ 275. H H

H CD₃ CD₃ 276. H H

H CD₃ CD₃ 277. H H

H CD₃ CD₃ 278. H H

H CD₃ CD₃ 279. H H

H CD₃ CD₃ 280. H H

H CD₃ CD₃ 281. H H

H CD₃ CD₃ 282. H H

H CD₃ CD₃ 283. H H

H CD₃ CD₃ 284. H H

H CD₃ CD₃ 285. H H

H CD₃ CD₃ 286. H H

H CD₃ CD₃ 287. CD₃ H CD₃ CD₃ CD₃ CD₃ 288. CD₃ H CD₂CD₃ CD₃ CD₃ CD₃ 289. CD₃ H CD₂CH₃ CD₃ CD₃ CD₃ 290. CD₃ H CD(CD₃)₂ CD₃ CD₃ CD₃ 291. CD₃ H CD(CH₃)₂ CD₃ CD₃ CD₃ 292. CD₃ H CD₂CD(CD₃)₂ CD₃ CD₃ CD₃ 293. CD₃ H CD₂CH(CH₃)₂ CD₃ CD₃ CD₃ 294. CD₃ H CD₂C(CD₃)₃ CD₃ CD₃ CD₃ 295. CD₃ H CD₂C(CH₃)₃ CD₃ CD₃ CD₃ 296. CD₃ H CD₂CD₂CF₃ CD₃ CD₃ CD₃ 297. CD₃ H CD₂CH₂CF₃ CD₃ CD₃ CD₃ 298. CD₃ H CD₂CCF₃(CH₃)₂ CD₃ CD₃ CD₃ 299. CD₃ H

CD₃ CD₃ CD₃ 300. CD₃ H

CD₃ CD₃ CD₃ 301. CD₃ H

CD₃ CD₃ CD₃ 302. CD₃ H

CD₃ CD₃ CD₃ 303. CD₃ H

CD₃ CD₃ CD₃ 304. CD₃ H

CD₃ CD₃ CD₃ 305. CD₃ H

CD₃ CD₃ CD₃ 306. CD₃ H

CD₃ CD₃ CD₃ 307. CD₃ H

CD₃ CD₃ CD₃ 308. CD₃ H

CD₃ CD₃ CD₃ 309. CD₃ H

CD₃ CD₃ CD₃ 310. CD₃ H

CD₃ CD₃ CD₃ 311. CD₃ H

CD₃ CD₃ CD₃ 312. CD₃ H

CD₃ CD₃ CD₃ 313. CD₃ H

CD₃ CD₃ CD₃ 314. CD₃ H

CD₃ CD₃ CD₃ 315. CD₃ H

CD₃ CD₃ CD₃ 316. CD₃ H

CD₃ CD₃ CD₃ 317. CD₃ H

CD₃ CD₃ CD₃ 318. CD₃ H

CD₃ CD₃ CD₃ 319. CH₃ CH₂CH₃ CH₃ CH₃ H CH₃ 320. CH₃ CH(CH₃)₂ CH₃ CH₃ CH₃ 321. CH₃ CH₂CH(CH₃)₂ CH₃ CH₃ H CH₃ 322. CH₃ C(CH₃)₃ CH₃ CH₃ CH₃ 323. CH₃ CH₂C(CH₃)₃ CH₃ CH₃ H CH₃ 324. CH₃ CH₂CH₂CF₃ CH₃ CH₃ CH₃ 325. CH₃ CH₂CCF₃(CH₃)₂ CH₃ CH₃ H CH₃ 326. CH₃

CH₃ CH₃ CH₃ 327. CH₃

CH₃ CH₃ H CH₃ 328. CH₃

CH₃ CH₃ CH₃ 329. CH₃

CH₃ CH₃ H CH₃ 330. CH₃

CH₃ CH₃ H CH₃ 331. CH₃

CH₃ CH₃ H CH₃ 332. CH₃

CH₃ CH₃ CH₃ 333. CH₃

CH₃ CH₃ H CH₃ 334. CH₃

CH₃ CH₃ CH₃ 335. CH₃

CH₃ CH₃ H CH₃ 336. CH₃

CH₃ CH₃ CH₃ 337. CH₃

CH₃ CH₃ H CH₃ 338. CH₃

CH₃ CH₃ CH₃ 339. CH₃

CH₃ CH₃ H CH₃ 340. CH₃

CH₃ CH₃ CH₃ 341. CH₃

CH₃ CH₃ H CH₃ 342. CH₃

CH₃ CH₃ CH₃ 343. CH₃

CH₃ CH₃ H CH₃ 344. CH₃

CH₃ CH₃ CH₃ 345. CH₃

CH₃ CH₃ H CH₃ 346. CD₃ CD₂CD₃ CD₃ CD₃ H CD₃ 347. CD₃ CD₂CH₃ CD₃ CD₃ CD₃ 348. CD₃ CD(CD₃)₂ CD₃ CD₃ H CD₃ 349. CD₃ CD(CH₃)₂ CD₃ CD₃ CD₃ 350. CD₃ CD₂CD(CD₃)₂ CD₃ CD₃ H CD₃ 351. CD₃ CD₂CH(CH₃)₂ CD₃ CD₃ CD₃ 352. CD₃ CD₂C(CD₃)₃ CD₃ CD₃ H CD₃ 353. CD₃ CD₂C(CH₃)₃ CD₃ CD₃ CD₃ 354. CD₃ CD₂CD₂CF₃ CD₃ CD₃ H CD₃ 355. CD₃ CD₂CH₂CF₃ CD₃ CD₃ CD₃ 356. CD₃ CD₂CCF₃(CH₃)₂ CD₃ CD₃ H CD₃ 357. CD₃

CD₃ CD₃ H CD₃ 358. CD₃

CD₃ CD₃ H CD₃ 359. CD₃

CD₃ CD₃ CD₃ 360. CD₃

CD₃ CD₃ H CD₃ 361. CD₃

CD₃ CD₃ CD₃ 362. CD₃

CD₃ CD₃ H CD₃ 363. CD₃

CD₃ CD₃ CD₃ 364. CD₃

CD₃ CD₃ H CD₃ 365. CD₃

CD₃ CD₃ CD₃ 366. CD₃

CD₃ CD₃ H CD₃ 367. CD₃

CD₃ CD₃ CD₃ 368. CD₃

CD₃ CD₃ H CD₃ 369. CD₃

CD₃ CD₃ CD₃ 370. CD₃

CD₃ CD₃ H CD₃ 371. CD₃

CD₃ CD₃ CD₃ 372. CD₃

CD₃ CD₃ H CD₃ 373. CD₃

CD₃ CD₃ CD₃ 374. CD₃

CD₃ CD₃ H CD₃ 375. CD₃

CD₃ CD₃ CD₃ 376. CD₃

CD₃ CD₃ H CD₃ 377. CD₃ CD₂CD₃ CD₃ CD₃ CD₂CD₃ CD₃ 378. CD₃ CD₂CH₃ CD₃ CD₃ CD₂CD₃ CD₃ 379. CD₃ CD(CD₃)₂ CD₃ CD₃ CD₂CD₃ CD₃ 380. CD₃ CD(CH₃)₂ CD₃ CD₃ CD₂CD₃ CD₃ 381. CD₃ CD₂CD(CD₃)₂ CD₃ CD₃ CD₂CD₃ CD₃ 382. CD₃ CD₂CH(CH₃)₂ CD₃ CD₃ CD₂CD₃ CD₃ 383. CD₃ CD₂C(CD₃)₃ CD₃ CD₃ CD₂CD₃ CD₃ 384. CD₃ CD₂C(CH₃)₃ CD₃ CD₃ CD₂CD₃ CD₃ 385. CD₃ CD₂CD₂CF₃ CD₃ CD₃ CD₂CD₃ CD₃ 386. CD₃ CD₂CH₂CF₃ CD₃ CD₃ CD₂CD₃ CD₃ 387. CD₃ CD₂CCF₃(CH₃)₂ CD₃ CD₃ CD₂CD₃ CD₃ 388. CD₃

CD₃ CD₃ CD₂CD₃ CD₃ 389. CD₃

CD₃ CD₃ CD₂CD₃ CD₃ 390. CD₃

CD₃ CD₃ CD₂CD₃ CD₃ 391. CD₃

CD₃ CD₃ CD₂CD₃ CD₃ 392. CD₃

CD₃ CD₃ CD₂CD₃ CD₃ 393. CD₃

CD₃ CD₃ CD₂CD₃ CD₃ 394. CD₃

CD₃ CD₃ CD₂CD₃ CD₃ 395. CD₃

CD₃ CD₃ CD₂CD₃ CD₃ 396. CD₃

CD₃ CD₃ CD₂CD₃ CD₃ 397. CD₃

CD₃ CD₃ CD₂CD₃ CD₃ 398. CD₃

CD₃ CD₃ CD₂CD₃ CD₃ 399. CD₃

CD₃ CD₃ CD₂CD₃ CD₃ 400. CD₃

CD₃ CD₃ CD₂CD₃ CD₃ 401. CD₃

CD₃ CD₃ CD₂CD₃ CD₃ 402. CD₃

CD₃ CD₃ CD₂CD₃ CD₃ 403. CD₃

CD₃ CD₃ CD₂CD₃ CD₃ 404. CD₃

CD₃ CD₃ CD₂CD₃ CD₃ 405. CD₃

CD₃ CD₃ CD₂CD₃ CD₃ 406. CD₃

CD₃ CD₃ CD₂CD₃ CD₃ 407. CD₃

CD₃ CD₃ CD₂CD₃ CD₃ 408. CH₃ CH₃ H H H CH₃ 409. CH₃ CH₂CH₃ H H H CH₃ 410. CH₃ CH(CH₃)₂ H H H CH₃ 411. CH₃ CH₂CH(CH₃)₂ H H H CH₃ 412. CH₃ C(CH₃)₃ H H H CH₃ 413. CH₃ CH₂C(CH₃)₃ H H H CH₃ 414. CH₃ CH₂CH₂CF₃ H H H CH₃ 415. CH₃ CH₂CCF₃(CH₃)₂ H H H CH₃ 416. CH₃

H H H CH₃ 417. CH₃

H H H CH₃ 418. CH₃

H H H CH₃ 419. CH₃

H H H CH₃ 420. CH₃

H H H CH₃ 421. CH₃

H H H CH₃ 422. CH₃

H H H CH₃ 423. CH₃

H H H CH₃ 424. CH₃

H H H CH₃ 425. CH₃

H H H CH₃ 426. CH₃

H H H CH₃ 427. CH₃

H H H CH₃ 428. CH₃

H H H CH₃ 429. CH₃

H H H CH₃ 430. CH₃

H H H CH₃ 431. CH₃

H H H CH₃ 432. CH₃

H H H CH₃ 433. CH₃

H H H CH₃ 434. CH₃

H H H CH₃ 435. CH₃

H H H CH₃ 436. CD₃ CD₃ H H H CD₂CD₃ 437. CD₃ CD₃ H H H CD₂CD₃ 438. CD₃ CD₂CH₃ H H H CD₂CD₃ 439. CD₃ CD(CD₃)₂ H H H CD₂CD₃ 440. CD₃ CD(CH₃)₂ H H H CD₂CD₃ 441. CD₃ CD₂CD(CD₃)₂ H H H CD₂CD₃ 442. CD₃ CD₂CH(CH₃)₂ H H H CD₂CD₃ 443. CD₃ CD₂C(CD₃)₃ H H H CD₂CD₃ 444. CD₃ CD₂C(CH₃)₃ H H H CD₂CD₃ 445. CD₃ CD₂CD₂CF₃ H H H CD₂CD₃ 446. CD₃ CD₂CH₂CF₃ H H H CD₂CD₃ 447. CD₃ CD₂CCF₃(CH₃)₂ H H H CD₂CD₃ 448. CD₃

H H H CD₂CD₃ 449. CD₃

H H H CD₂CD₃ 450. CD₃

H H H CD₂CD₃ 451. CD₃

H H H CD₂CD₃ 452. CD₃

H H H CD₂CD₃ 453. CD₃

H H H CD₂CD₃ 454. CD₃

H H H CD₂CD₃ 455. CD₃

H H H CD₂CD₃ 456. CD₃

H H H CD₂CD₃ 457. CD₃

H H H CD₂CD₃ 458. CD₃

H H H CD₂CD₃ 459. CD₃

H H H CD₂CD₃ 460. CD₃

H H H CD₂CD₃ 461. CD₃

H H H CD₂CD₃ 462. CD₃

H H H CD₂CD₃ 463. CD₃

H H H CD₂CD₃ 464. CD₃

H H H CD₂CD₃ 465. CD₃

H H H CD₂CD₃ 466. CD₃

H H H CD₂CD₃ 467. CD₃

H H H CD₂CD₃ 468. CH₃ H CH₃ H H CH₃ 469. CH₃ H CH₂CH₃ H H CH₃ 470. CH₃ H CH(CH₃)₂ H H CH₃ 471. CH₃ H CH₂CH(CH₃)₂ H H CH₃ 472. CH₃ H C(CH₃)₃ H H CH₃ 473. CH₃ H CH₂C(CH₃)₃ H H CH₃ 474. CH₃ H CH₂CH₂CF₃ H H CH₃ 475. CH₃ H CH₂CCF₃(CH₃)₂ H H CH₃ 476. CH₃ H

H H CH₃ 477. CH₃ H

H H CH₃ 478. CH₃ H

H H CH₃ 479. CH₃ H

H H CH₃ 480. CH₃ H

H H CH₃ 481. CH₃ H

H H CH₃ 482. CH₃ H

H H CH₃ 483. CH₃ H

H H CH₃ 484. CH₃ H

H H CH₃ 485. CH₃ H

H H CH₃ 486. CH₃ H

H H CH₃ 487. CH₃ H

H H CH₃ 488. CH₃ H

H H CH₃ 489. CH₃ H

H H CH₃ 490. CH₃ H

H H CH₃ 491. CH₃ H

H H CH₃ 492. CH₃ H

H H CH₃ 493. CH₃ H

H H CH₃ 494. CH₃ H

H H CH₃ 495. CH₃ H

H H CH₃ 496. CD₃ H CD₃ H H CD₂CD₃ 497. CD₃ H CD₂CD₃ H H CD₂CD₃ 498. CD₃ H CD₂CH₃ H H CD₂CD₃ 499. CD₃ H CD(CD₃)₂ H H CD₂CD₃ 500. CD₃ H CD(CH₃)₂ H H CD₂CD₃ 501. CD₃ H CD₂CD(CD₃)₂ H H CD₂CD₃ 502. CD₃ H CD₂CH(CH₃)₂ H H CD₂CD₃ 503. CD₃ H CD₂C(CD₃)₃ H H CD₂CD₃ 504. CD₃ H CD₂C(CH₃)₃ H H CD₂CD₃ 505. CD₃ H CD₂CD₂CF₃ H H CD₂CD₃ 506. CD₃ H CD₂CH₂CF₃ H H CD₂CD₃ 507. CD₃ H CD₂CCF₃(CH₃)₂ H H CD₂CD₃ 508. CD₃ H

H H CD₂CD₃ 509. CD₃ H

H H CD₂CD₃ 510. CD₃ H

H H CD₂CD₃ 511. CD₃ H

H H CD₂CD₃ 512. CD₃ H

H H CD₂CD₃ 513. CD₃ H

H H CD₂CD₃ 514. CD₃ H

H H CD₂CD₃ 515. CD₃ H

H H CD₂CD₃ 516. CD₃ H

H H CD₂CD₃ 517. CD₃ H

H H CD₂CD₃ 518. CD₃ H

H H CD₂CD₃ 519. CD₃ H

H H CD₂CD₃ 520. CD₃ H

H H CD₂CD₃ 521. CD₃ H

H H CD₂CD₃ 522. CD₃ H

H H CD₂CD₃ 523. CD₃ H

H H CD₂CD₃ 524. CD₃ H

H H CD₂CD₃ 525. CD₃ H

H H CD₂CD₃ 526. CD₃ H

H H CD₂CD₃ 527. CD₃ H

H H CD₂CD₃ 528. CH(CH₃)₂ H H CH₃ CH₃ CH₃ 529. CH(CH₃)₂ H H CH₂CH₃ CH₃ CH₃ 530. CH(CH₃)₂ H H CH(CH₃)₂ CH₃ CH₃ 531. CH(CH₃)₂ H H CH₂CH(CH₃)₂ CH₃ CH₃ 532. CH(CH₃)₂ H H C(CH₃)₃ CH₃ CH₃ 533. CH(CH₃)₂ H H CH₂C(CH₃)₃ CH₃ CH₃ 534. CH(CH₃)₂ H H CH₂CH₂CF₃ CH₃ CH₃ 535. CH(CH₃)₂ H H CH₂CCF₃(CH₃)₂ CH₃ CH₃ 536. CH(CH₃)₂ H H

CH₃ CH₃ 537. CH(CH₃)₂ H H

CH₃ CH₃ 538. CH(CH₃)₂ H H

CH₃ CH₃ 539. CH(CH₃)₂ H H

CH₃ CH₃ 540. CH(CH₃)₂ H H

CH₃ CH₃ 541. CH(CH₃)₂ H H

CH₃ CH₃ 542. CH(CH₃)₂ H H

CH₃ CH₃ 543. CH(CH₃)₂ H H

CH₃ CH₃ 544. CH(CH₃)₂ H H

CH₃ CH₃ 545. CH(CH₃)₂ H H

CH₃ CH₃ 546. CH(CH₃)₂ H H

CH₃ CH₃ 547. CH(CH₃)₂ H H

CH₃ CH₃ 548. CH(CH₃)₂ H H

CH₃ CH₃ 549. CH(CH₃)₂ H H

CH₃ CH₃ 550. CH(CH₃)₂ H H

CH₃ CH₃ 551. CH(CH₃)₂ H H

CH₃ CH₃ 552. CH(CH₃)₂ H H

CH₃ CH₃ 553. CH(CH₃)₂ H H

CH₃ CH₃ 554. CH(CH₃)₂ H H

CH₃ CH₃ 555. CH(CH₃)₂ H H

CH₃ CH₃ 556. CD₃ H H CD₃ CD₃ CD₃ 557. CD₃ H H CD₂CD₃ CD₃ CD₃ 558. CD₃ H H CD₂CH₃ CD₃ CD₃ 559. CD₃ H H CD(CD₃)₂ CD₃ CD₃ 560. CD₃ H H CD(CH₃)₂ CD₃ CD₃ 561. CD₃ H H CD₂CD(CD₃)₂ CD₃ CD₃ 562. CD₃ H H CD₂CH(CH₃)₂ CD₃ CD₃ 563. CD₃ H H CD₂C(CD₃)₃ CD₃ CD₃ 564. CD₃ H H CD₂C(CH₃)₃ CD₃ CD₃ 565. CD₃ H H CD₂CD₂CF₃ CD₃ CD₃ 566. CD₃ H H CD₂CH₂CF₃ CD₃ CD₃ 567. CD₃ H H CD₂CCF₃(CH₃)₂ CD₃ CD₃ 568. CD₃ H H

CD₃ CD₃ 569. CD₃ H H

CD₃ CD₃ 570. CD₃ H H

CD₃ CD₃ 571. CD₃ H H

CD₃ CD₃ 572. CD₃ H H

CD₃ CD₃ 573. CD₃ H H

CD₃ CD₃ 574. CD₃ H H

CD₃ CD₃ 575. CD₃ H H

CD₃ CD₃ 576. CD₃ H H

CD₃ CD₃ 577. CD₃ H H

CD₃ CD₃ 578. CD₃ H H

CD₃ CD₃ 579. CD₃ H H

CD₃ CD₃ 580. CD₃ H H

CD₃ CD₃ 581. CD₃ H H

CD₃ CD₃ 582. CD₃ H H

CD₃ CD₃ 583. CD₃ H H

CD₃ CD₃ 584. CD₃ H H

CD₃ CD₃ 585. CD₃ H H

CD₃ CD₃ 586. CD₃ H H

CD₃ CD₃ 587. CD₃ H H

CD₃ CD₃ 588. H CH₃ CH₃ H CH₃ CH₃ 589. H CH₂CH₃ CH₃ H CH₃ CH₃ 590. H CH(CH₃)₂ CH₃ H CH₃ CH₃ 591. H CH₂CH(CH₃)₂ CH₃ H CH₃ CH₃ 592. H C(CH₃)₃ CH₃ H CH₃ CH₃ 593. H CH₂C(CH₃)₃ CH₃ H CH₃ CH₃ 594. H CH₂CH₂CF₃ CH₃ H CH₃ CH₃ 595. H CH₂CCF₃(CH₃)₂ CH₃ H CH₃ CH₃ 596. H

CH₃ H CH₃ CH₃ 597. H

CH₃ H CH₃ CH₃ 598. H

CH₃ H CH₃ CH₃ 599. H

CH₃ H CH₃ CH₃ 600. H

CH₃ H CH₃ CH₃ 601. H

CH₃ H CH₃ CH₃ 602. H

CH₃ H CH₃ CH₃ 603. H

CH₃ H CH₃ CH₃ 604. H

CH₃ H CH₃ CH₃ 605. H

CH₃ H CH₃ CH₃ 606. H

CH₃ H CH₃ CH₃ 607. H

CH₃ H CH₃ CH₃ 608. H

CH₃ H CH₃ CH₃ 609. H

CH₃ H CH₃ CH₃ 610. H

CH₃ H CH₃ CH₃ 611. H

CH₃ H CH₃ CH₃ 612. H

CH₃ H CH₃ CH₃ 613. H

CH₃ H CH₃ CH₃ 614. H

CH₃ H CH₃ CH₃ 615. H

CH₃ H CH₃ CH₃ 616. CD₃ CD₃ CD₃ H CD₃ CD₃ 617. CD₃ CD₂CD₃ CD₃ H CD₃ CD₃ 618. CD₃ CD₂CH₃ CD₃ H CD₃ CD₃ 619. CD₃ CD(CD₃)₂ CD₃ H CD₃ CD₃ 620. CD₃ CD(CH₃)₂ CD₃ H CD₃ CD₃ 621. CD₃ CD₂CD(CD₃)₂ CD₃ H CD₃ CD₃ 622. CD₃ CD₂CH(CH₃)₂ CD₃ H CD₃ CD₃ 623. CD₃ CD₂C(CD₃)₃ CD₃ H CD₃ CD₃ 624. CD₃ CD₂C(CH₃)₃ CD₃ H CD₃ CD₃ 625. CD₃ CD₂CD₂CF₃ CD₃ H CD₃ CD₃ 626. CD₃ CD₂CH₂CF₃ CD₃ H CD₃ CD₃ 627. CD₃ CD₂CCF₃(CH₃)₂ CD₃ H CD₃ CD₃ 628. CD₃

CD₃ H CD₃ CD₃ 629. CD₃

CD₃ H CD₃ CD₃ 630. CD₃

CD₃ H CD₃ CD₃ 631. CD₃

CD₃ H CD₃ CD₃ 632. CD₃

CD₃ H CD₃ CD₃ 633. CD₃

CD₃ H CD₃ CD₃ 634. CD₃

CD₃ H CD₃ CD₃ 635. CD₃

CD₃ H CD₃ CD₃ 636. CD₃

CD₃ H CD₃ CD₃ 637. CD₃

CD₃ H CD₃ CD₃ 638. CD₃

CD₃ H CD₃ CD₃ 639. CD₃

CD₃ H CD₃ CD₃ 640. CD₃

CD₃ H CD₃ CD₃ 641. CD₃

CD₃ H CD₃ CD₃ 642. CD₃

CD₃ H CD₃ CD₃ 643. CD₃

CD₃ H CD₃ CD₃ 644. CD₃

CD₃ H CD₃ CD₃ 645. CD₃

CD₃ H CD₃ CD₃ 646. CD₃

CD₃ H CD₃ CD₃ 647. CD₃

CD₃ H CD₃ CD₃ 648. CH₃ CH₃ CH₂CH₃ H CH₃ CH₂CH₃ 649. CH₃ CH₃ CH(CH₃)₂ H CH₃ CH₂CH₃ 650. CH₃ CH₃ CH₂CH(CH₃)₂ H CH₃ CH₂CH₃ 651. CH₃ CH₃ C(CH₃)₃ H CH₃ CH₂CH₃ 652. CH₃ CH₃ CH₂C(CH₃)₃ H CH₃ CH₂CH₃ 653. CH₃ CH₃ CH₂CH₂CF₃ H CH₃ CH₂CH₃ 654. CH₃ CH₃ CH₂CCF₃(CH₃)₂ H CH₃ CH₂CH₃ 655. CH₃ CH₃

H CH₃ CH₂CH₃ 656. CH₃ CH₃

H CH₃ CH₂CH₃ 657. CH₃ CH₃

H CH₃ CH₂CH₃ 658. CH₃ CH₃

H CH₃ CH₂CH₃ 659. CH₃ CH₃

H CH₃ CH₂CH₃ 660. CH₃ CH₃

H CH₃ CH₂CH₃ 661. CH₃ CH₃

H CH₃ CH₂CH₃ 662. CH₃ CH₃

H CH₃ CH₂CH₃ 663. CH₃ CH₃

H CH₃ CH₂CH₃ 664. CH₃ CH₃

H CH₃ CH₂CH₃ 665. CH₃ CH₃

H CH₃ CH₂CH₃ 666. CH₃ CH₃

H CH₃ CH₂CH₃ 667. CH₃ CH₃

H CH₃ CH₂CH₃ 668. CH₃ CH₃

H CH₃ CH₂CH₃ 669. CH₃ CH₃

H CH₃ CH₂CH₃ 670. CH₃ CH₃

H CH₃ CH₂CH₃ 671. CH₃ CH₃

H CH₃ CH₂CH₃ 672. CH₃ CH₃

H CH₃ CH₂CH₃ 673. CH₃ CH₃

H CH₃ CH₂CH₃ 674. CH₃ CH₃

H CH₃ CH₂CH₃ 675. CD₃ CD₃ CD₂CD₃ H CD₂CH₃ CD₂CH₃ 676. CD₃ CD₃ CD₂CH₃ H CD₂CH₃ CD₂CH₃ 677. CD₃ CD₃ CD(CD₃)₂ H CD₂CH₃ CD₂CH₃ 678. CD₃ CD₃ CD(CH₃)₂ H CD₂CH₃ CD₂CH₃ 679. CD₃ CD₃ CD₂CD(CD₃)₂ H CD₂CH₃ CD₂CH₃ 680. CD₃ CD₃ CD₂CH(CH₃)₂ H CD₂CH₃ CD₂CH₃ 681. CD₃ CD₃ CD₂C(CD₃)₃ H CD₂CH₃ CD₂CH₃ 682. CD₃ CD₃ CD₂C(CH₃)₃ H CD₂CH₃ CD₂CH₃ 683. CD₃ CD₃ CD₂CD₂CF₃ H CD₂CH₃ CD₂CH₃ 684. CD₃ CD₃ CD₂CH₂CF₃ H CD₂CH₃ CD₂CH₃ 685. CD₃ CD₃ CD₂CCF₃(CH₃)₂ H CD₂CH₃ CD₂CH₃ 686. CD₃ CD₃

H CD₂CH₃ CD₂CH₃ 687. CD₃ CD₃

H CD₂CH₃ CD₂CH₃ 688. CD₃ CD₃

H CD₂CH₃ CD₂CH₃ 689. CD₃ CD₃

H CD₂CH₃ CD₂CH₃ 690. CD₃ CD₃

H CD₂CH₃ CD₂CH₃ 691. CD₃ CD₃

H CD₂CH₃ CD₂CH₃ 692. CD₃ CD₃

H CD₂CH₃ CD₂CH₃ 693. CD₃ CD₃

H CD₂CH₃ CD₂CH₃ 694. CD₃ CD₃

H CD₂CH₃ CD₂CH₃ 695. CD₃ CD₃

H CD₂CH₃ CD₂CH₃ 696. CD₃ CD₃

H CD₂CH₃ CD₂CH₃ 697. CD₃ CD₃

H CD₂CH₃ CD₂CH₃ 698. CD₃ CD₃

H CD₂CH₃ CD₂CH₃ 699. CD₃ CD₃

H CD₂CH₃ CD₂CH₃ 700. CD₃ CD₃

H CD₂CH₃ CD₂CH₃ 701. CD₃ CD₃

H CD₂CH₃ CD₂CH₃ 702. CD₃ CD₃

H CD₂CH₃ CD₂CH₃ 703. CD₃ CD₃

H CD₂CH₃ CD₂CH₃ 704. CD₃ CD₃

H CD₂CH₃ CD₂CH₃ 705. CD₃ CD₃

H CD₂CH₃ CD₂CH₃ 706. H CH₃ CH₃ CH₃ CH₂CH₃ CH₂CH₃ 707. H CH₃ CH₂CH₃ CH₃ CH₂CH₃ CH₂CH₃ 708. H CH₃ CH(CH₃)₂ CH₃ CH₂CH₃ CH₂CH₃ 709. H CH₃ CH₂CH(CH₃)₂ CH₃ CH₂CH₃ CH₂CH₃ 710. H CH₃ C(CH₃)₃ CH₃ CH₂CH₃ CH₂CH₃ 711. H CH₃ CH₂C(CH₃)₃ CH₃ CH₂CH₃ CH₂CH₃ 712. H CH₃ CH₂CH₂CF₃ CH₃ CH₂CH₃ CH₂CH₃ 713. H CH₃ CH₂CCF₃(CH₃)₂ CH₃ CH₂CH₃ CH₂CH₃ 714. H CH₃

CH₃ CH₂CH₃ CH₂CH₃ 715. H CH₃

CH₃ CH₂CH₃ CH₂CH₃ 716. H CH₃

CH₃ CH₂CH₃ CH₂CH₃ 717. H CH₃

CH₃ CH₂CH₃ CH₂CH₃ 718. H CH₃

CH₃ CH₂CH₃ CH₂CH₃ 719. H CH₃

CH₃ CH₂CH₃ CH₂CH₃ 720. H CH₃

CH₃ CH₂CH₃ CH₂CH₃ 721. H CH₃

CH₃ CH₂CH₃ CH₂CH₃ 722. H CH₃

CH₃ CH₂CH₃ CH₂CH₃ 723. H CH₃

CH₃ CH₂CH₃ CH₂CH₃ 724. H CH₃

CH₃ CH₂CH₃ CH₂CH₃ 725. H CH₃

CH₃ CH₂CH₃ CH₂CH₃ 726. H CH₃

CH₃ CH₂CH₃ CH₂CH₃ 727. H CH₃

CH₃ CH₂CH₃ CH₂CH₃ 728. H CH₃

CH₃ CH₂CH₃ CH₂CH₃ 729. H CH₃

CH₃ CH₂CH₃ CH₂CH₃ 730. H CH₃

CH₃ CH₂CH₃ CH₂CH₃ 731. H CH₃

CH₃ CH₂CH₃ CH₂CH₃ 732. H CH₃

CH₃ CH₂CH₃ CH₂CH₃ 733. H CH₃

CH₃ CH₂CH₃ CH₂CH₃ 734. CD₃ CD₃ CD₃ CD₃ CD₂CH₃ CD₂CH₃ 735. CD₃ CD₃ CD₂CD₃ CD₃ CD₂CH₃ CD₂CH₃ 736. CD₃ CD₃ CD₂CH₃ CD₃ CD₂CH₃ CD₂CH₃ 737. CD₃ CD₃ CD(CD₃)₂ CD₃ CD₂CH₃ CD₂CH₃ 738. CD₃ CD₃ CD(CH₃)₂ CD₃ CD₂CH₃ CD₂CH₃ 739. CD₃ CD₃ CD₂CD(CD₃)₂ CD₃ CD₂CH₃ CD₂CH₃ 740. CD₃ CD₃ CD₂CH(CH₃)₂ CD₃ CD₂CH₃ CD₂CH₃ 741. CD₃ CD₃ CD₂C(CD₃)₃ CD₃ CD₂CH₃ CD₂CH₃ 742. CD₃ CD₃ CD₂C(CH₃)₃ CD₃ CD₂CH₃ CD₂CH₃ 743. CD₃ CD₃ CD₂CD₂CF₃ CD₃ CD₂CH₃ CD₂CH₃ 744. CD₃ CD₃ CD₂CH₂CF₃ CD₃ CD₂CH₃ CD₂CH₃ 745. CD₃ CD₃ CD₂CCF₃(CH₃)₂ CD₃ CD₂CH₃ CD₂CH₃ 746. CD₃ CD₃

CD₃ CD₂CH₃ CD₂CH₃ 747. CD₃ CD₃

CD₃ CD₂CH₃ CD₂CH₃ 748. CD₃ CD₃

CD₃ CD₂CH₃ CD₂CH₃ 749. CD₃ CD₃

CD₃ CD₂CH₃ CD₂CH₃ 750. CD₃ CD₃

CD₃ CD₂CH₃ CD₂CH₃ 751. CD₃ CD₃

CD₃ CD₂CH₃ CD₂CH₃ 752. CD₃ CD₃

CD₃ CD₂CH₃ CD₂CH₃ 753. CD₃ CD₃

CD₃ CD₂CH₃ CD₂CH₃ 754. CD₃ CD₃

CD₃ CD₂CH₃ CD₂CH₃ 755. CD₃ CD₃

CD₃ CD₂CH₃ CD₂CH₃ 756. CD₃ CD₃

CD₃ CD₂CH₃ CD₂CH₃ 757. CD₃ CD₃

CD₃ CD₂CH₃ CD₂CH₃ 758. CD₃ CD₃

CD₃ CD₂CH₃ CD₂CH₃ 759. CD₃ CD₃

CD₃ CD₂CH₃ CD₂CH₃ 760. CD₃ CD₃

CD₃ CD₂CH₃ CD₂CH₃ 761. CD₃ CD₃

CD₃ CD₂CH₃ CD₂CH₃ 762. CD₃ CD₃

CD₃ CD₂CH₃ CD₂CH₃ 763. CD₃ CD₃

CD₃ CD₂CH₃ CD₂CH₃ 764. CD₃ CD₃

CD₃ CD₂CH₃ CD₂CH₃ 765. CD₃ CD₃

CD₃ CD₂CH₃ CD₂CH₃ 766. CH₃ CH₂CH₃ CH₃ CH₂CH₃ H CH₂CH₃ 767. CH₃ CH(CH₃)₂ CH₃ CH(CH₃)₂ H CH₂CH₃ 768. CH₃ CH₂CH(CH₃)₂ CH₃ CH₂CH(CH₃)₂ H CH₂CH₃ 769. CH₃ C(CH₃)₃ CH₃ C(CH₃)₃ H CH₂CH₃ 770. CH₃ CH₂C(CH₃)₃ CH₃ CH₂C(CH₃)₃ H CH₂CH₃ 771. CH₃ CH₂CH₂CF₃ CH₃ CH₂CH₂CF₃ H CH₂CH₃ 772. CH₃ CH₂CCF₃(CH₃)₂ CH₃ CH₂CCF₃(CH₃)₂ H CH₂CH₃ 773. CH₃

CH₃

H CH₂CH₃ 774. CH₃

CH₃

H CH₂CH₃ 775. CH₃

CH₃

H CH₂CH₃ 776. CH₃

CH₃

H CH₂CH₃ 777. CH₃

CH₃

H CH₂CH₃ 778. CH₃

CH₃

H CH₂CH₃ 779. CH₃

CH₃

H CH₂CH₃ 780. CH₃

CH₃

H CH₂CH₃ 781. CH₃

CH₃

H CH₂CH₃ 782. CH₃

CH₃

H CH₂CH₃ 783. CH₃

CH₃

H CH₂CH₃ 784. CH₃

CH₃

H CH₂CH₃ 785. CH₃

CH₃

H CH₂CH₃ 786. CH₃

CH₃

H CH₂CH₃ 787. CH₃

CH₃

H CH₂CH₃ 788. CH₃

CH₃

H CH₂CH₃ 789. CH₃

CH₃

H CH₂CH₃ 790. CH₃

CH₃

H CH₂CH₃ 791. CH₃

CH₃

H CH₂CH₃ 792. CH₃

CH₃

H CH₂CH₃ 793. CD₃ CD₂CD₃ CD₃ CD₂CD₃ H CD₂CH₃ 794. CD₃ CD₂CH₃ CD₃ CD₂CH₃ H CD₂CH₃ 795. CD₃ CD(CD₃)₂ CD₃ CD(CD₃)₂ H CD₂CH₃ 796. CD₃ CD(CH₃)₂ CD₃ CD(CH₃)₂ H CD₂CH₃ 797. CD₃ CD₂CD(CD₃)₂ CD₃ CD₂CD(CD₃)₂ H CD₂CH₃ 798. CD₃ CD₂CH(CH₃)₂ CD₃ CD₂CH(CH₃)₂ H CD₂CH₃ 799. CD₃ CD₂C(CD₃)₃ CD₃ CD₂C(CD₃)₃ H CD₂CH₃ 800. CD₃ CD₂C(CH₃)₃ CD₃ CD₂C(CH₃)₃ H CD₂CH₃ 801. CD₃ CD₂CD₂CF₃ CD₃ CD₂CD₂CF₃ H CD₂CH₃ 802. CD₃ CD₂CH₂CF₃ CD₃ CD₂CH₂CF₃ H CD₂CH₃ 803. CD₃ CD₂CCF₃(CH₃)₂ CD₃ CD₂CCF₃(CH₃)₂ H CD₂CH₃ 804. CD₃

CD₃

H CD₂CH₃ 805. CD₃

CD₃

H CD₂CH₃ 806. CD₃

CD₃

H CD₂CH₃ 807. CD₃

CD₃

H CD₂CH₃ 808. CD₃

CD₃

H CD₂CH₃ 809. CD₃

CD₃

H CD₂CH₃ 810. CD₃

CD₃

H CD₂CH₃ 811. CD₃

CD₃

H CD₂CH₃ 812. CD₃

CD₃

H CD₂CH₃ 813. CD₃

CD₃

H CD₂CH₃ 814. CD₃

CD₃

H CD₂CH₃ 815. CD₃

CD₃

H CD₂CH₃ 816. CD₃

CD₃

H CD₂CH₃ 817. CD₃

CD₃

H CD₂CH₃ 818. CD₃

CD₃

H CD₂CH₃ 819. CD₃

CD₃

H CD₂CH₃ 820. CD₃

CD₃

H CD₂CH₃ 821. CD₃

CD₃

H CD₂CH₃ 822. CD₃

CD₃

H CD₂CH₃ 823. CD₃

CD₃

H CD₂CH₃ 824. CH₂CH₃ CH₃ H H H CH(CH₃)₂ 825. CH₂CH₃ CH₂CH₃ H H H CH(CH₃)₂ 826. CH₂CH₃ CH(CH₃)₂ H H H CH(CH₃)₂ 827. CH₂CH₃ CH₂CH(CH₃)₂ H H H CH(CH₃)₂ 828. CH₂CH₃ C(CH₃)₃ H H H CH(CH₃)₂ 829. CH₂CH₃ CH₂C(CH₃)₃ H H H CH(CH₃)₂ 830. CH₂CH₃ CH₂CH₂CF₃ H H H CH(CH₃)₂ 831. CH₂CH₃ CH₂CCF₃(CH₃)₂ H H H CH(CH₃)₂ 832. CH₂CH₃

H H H CH(CH₃)₂ 833. CH₂CH₃

H H H CH(CH₃)₂ 834. CH₂CH₃

H H H CH(CH₃)₂ 835. CH₂CH₃

H H H CH(CH₃)₂ 836. CH₂CH₃

H H H CH(CH₃)₂ 837. CH₂CH₃

H H H CH(CH₃)₂ 838. CH₂CH₃

H H H CH(CH₃)₂ 839. CH₂CH₃

H H H CH(CH₃)₂ 840. CH₂CH₃

H H H CH(CH₃)₂ 841. CH₂CH₃

H H H CH(CH₃)₂ 842. CH₂CH₃

H H H CH(CH₃)₂ 843. CH₂CH₃

H H H CH(CH₃)₂ 844. CH₂CH₃

H H H CH(CH₃)₂ 845. CH₂CH₃

H H H CH(CH₃)₂ 846. CH₂CH₃

H H H CH(CH₃)₂ 847. CH₂CH₃

H H H CH(CH₃)₂ 848. CH₂CH₃

H H H CH(CH₃)₂ 849. CH₂CH₃

H H H CH(CH₃)₂ 850. CH₂CH₃

H H H CH(CH₃)₂ 851. CH₂CH₃

H H H CH(CH₃)₂ 852. CD₂CH₃ CD₃ H H CD₂CH₃ CD₂CH₃ 853. CD₂CH₃ CD₂CD₃ H H CD₂CH₃ CD₂CH₃ 854. CD₂CH₃ CD₂CH₃ H H CD₂CH₃ CD₂CH₃ 855. CD₂CH₃ CD(CD₃)₂ H H CD₂CH₃ CD₂CH₃ 856. CD₂CH₃ CD(CH₃)₂ H H CD₂CH₃ CD₂CH₃ 857. CD₂CH₃ CD₂CD(CD₃)₂ H H CD₂CH₃ CD₂CH₃ 858. CD₂CH₃ CD₂CH(CH₃)₂ H H CD₂CH₃ CD₂CH₃ 859. CD₂CH₃ CD₂C(CD₃)₃ H H CD₂CH₃ CD₂CH₃ 860. CD₂CH₃ CD₂C(CH₃)₃ H H CD₂CH₃ CD₂CH₃ 861. CD₂CH₃ CD₂CD₂CF₃ H H CD₂CH₃ CD₂CH₃ 862. CD₂CH₃ CD₂CH₂CF₃ H H CD₂CH₃ CD₂CH₃ 863. CD₂CH₃ CD₂CCF₃(CH₃)₂ H H CD₂CH₃ CD₂CH₃ 864. CD₂CH₃

H H CD₂CH₃ CD₂CH₃ 865. CD₂CH₃

H H CD₂CH₃ CD₂CH₃ 866. CD₂CH₃

H H CD₂CH₃ CD₂CH₃ 867. CD₂CH₃

H H CD₂CH₃ CD₂CH₃ 868. CD₂CH₃

H H CD₂CH₃ CD₂CH₃ 869. CD₂CH₃

H H CD₂CH₃ CD₂CH₃ 870. CD₂CH₃

H H CD₂CH₃ CD₂CH₃ 871. CD₂CH₃

H H CD₂CH₃ CD₂CH₃ 872. CD₂CH₃

H H CD₂CH₃ CD₂CH₃ 873. CD₂CH₃

H H CD₂CH₃ CD₂CH₃ 874. CD₂CH₃

H H CD₂CH₃ CD₂CH₃ 875. CD₂CH₃

H H CD₂CH₃ CD₂CH₃ 876. CD₂CH₃

H H CD₂CH₃ CD₂CH₃ 877. CD₂CH₃

H H CD₂CH₃ CD₂CH₃ 878. CD₂CH₃

H H CD₂CH₃ CD₂CH₃ 879. CD₂CH₃

H H CD₂CH₃ CD₂CH₃ 880. CD₂CH₃

H H CD₂CH₃ CD₂CH₃ 881. CD₂CH₃

H H CD₂CH₃ CD₂CH₃ 882. CD₂CH₃

H H CD₂CH₃ CD₂CH₃ 883. CD₂CH₃

H H CD₂CH₃ CD₂CH₃ 884. CD₂CD₃ CD₃ H H H CD(CH₃)₂ 885. CD₂CD₃ CD₂CD₃ H H H CD(CH₃)₂ 886. CD₂CD₃ CD₂CH₃ H H H CD(CH₃)₂ 887. CD₂CD₃ CD(CD₃)₂ H H H CD(CH₃)₂ 888. CD₂CD₃ CD(CH₃)₂ H H H CD(CH₃)₂ 889. CD₂CD₃ CD₂CD(CD₃)₂ H H H CD(CH₃)₂ 890. CD₂CD₃ CD₂CH(CH₃)₂ H H H CD(CH₃)₂ 891. CD₂CD₃ CD₂C(CD₃)₃ H H H CD(CH₃)₂ 892. CD₂CD₃ CD₂C(CH₃)₃ H H H CD(CH₃)₂ 893. CD₂CD₃ CD₂CD₂CF₃ H H H CD(CH₃)₂ 894. CD₂CD₃ CD₂CH₂CF₃ H H H CD(CH₃)₂ 895. CD₂CD₃ CD₂CCF₃(CH₃)₂ H H H CD(CH₃)₂ 896. CD₂CD₃

H H H CD(CH₃)₂ 897. CD₂CD₃

H H H CD(CH₃)₂ 898. CD₂CD₃

H H H CD(CH₃)₂ 899. CD₂CD₃

H H H CD(CH₃)₂ 900. CD₂CD₃

H H H CD(CH₃)₂ 901. CD₂CD₃

H H H CD(CH₃)₂ 902. CD₂CD₃

H H H CD(CH₃)₂ 903. CD₂CD₃

H H H CD(CH₃)₂ 904. CD₂CD₃

H H H CD(CH₃)₂ 905. CD₂CD₃

H H H CD(CH₃)₂ 906. CD₂CD₃

H H H CD(CH₃)₂ 907. CD₂CD₃

H H H CD(CH₃)₂ 908. CD₂CD₃

H H H CD(CH₃)₂ 909. CD₂CD₃

H H H CD(CH₃)₂ 910. CD₂CD₃

H H H CD(CH₃)₂ 911. CD₂CD₃

H H H CD(CH₃)₂ 912. CD₂CD₃

H H H CD(CH₃)₂ 913. CD₂CD₃

H H H CD(CH₃)₂ 914. CD₂CD₃

H H H CD(CH₃)₂ 915. CD₂CD₃

H H H CD(CH₃)₂ 916. CH₂CH₃ H CH₂CH₃ H CH₂CH₃ CH₂CH₃ 917. CH₂CH₃ H CH(CH₃)₂ H CH₂CH₃ CH₂CH₃ 918. CH₂CH₃ H CH₂CH(CH₃)₂ H CH₂CH₃ CH₂CH₃ 919. CH₂CH₃ H C(CH₃)₃ H CH₂CH₃ CH₂CH₃ 920. CH₂CH₃ H CH₂C(CH₃)₃ H CH₂CH₃ CH₂CH₃ 921. CH₂CH₃ H CH₂CH₂CF₃ H CH₂CH₃ CH₂CH₃ 922. CH₂CH₃ H CH₂CCF₃(CH₃)₂ H CH₂CH₃ CH₂CH₃ 923. CH₂CH₃ H

H CH₂CH₃ CH₂CH₃ 924. CH₂CH₃ H

H CH₂CH₃ CH₂CH₃ 925. CH₂CH₃ H

H CH₂CH₃ CH₂CH₃ 926. CH₂CH₃ H

H CH₂CH₃ CH₂CH₃ 927. CH₂CH₃ H

H CH₂CH₃ CH₂CH₃ 928. CH₂CH₃ H

H CH₂CH₃ CH₂CH₃ 929. CH₂CH₃ H

H CH₂CH₃ CH₂CH₃ 930. CH₂CH₃ H

H CH₂CH₃ CH₂CH₃ 931. CH₂CH₃ H

H CH₂CH₃ CH₂CH₃ 932. CH₂CH₃ H

H CH₂CH₃ CH₂CH₃ 933. CH₂CH₃ H

H CH₂CH₃ CH₂CH₃ 934. CH₂CH₃ H

H CH₂CH₃ CH₂CH₃ 935. CH₂CH₃ H

H CH₂CH₃ CH₂CH₃ 936. CH₂CH₃ H

H CH₂CH₃ CH₂CH₃ 937. CH₂CH₃ H

H CH₂CH₃ CH₂CH₃ 938. CH₂CH₃ H

H CH₂CH₃ CH₂CH₃ 939. CH₂CH₃ H

H CH₂CH₃ CH₂CH₃ 940. CH₂CH₃ H

H CH₂CH₃ CH₂CH₃ 941. CH₂CH₃ H

H CH₂CH₃ CH₂CH₃ 942. CH₂CH₃ H

H CH₂CH₃ CH₂CH₃ 943. CD₂CH₃ H CD₃ H CD(CH₃)₂ CD(CH₃)₂ 944. CD₂CH₃ H CD₂CD₃ H CD(CH₃)₂ CD(CH₃)₂ 945. CD₂CH₃ H CD₂CH₃ H CD(CH₃)₂ CD(CH₃)₂ 946. CD₂CH₃ H CD(CD₃)₂ H CD(CH₃)₂ CD(CH₃)₂ 947. CD₂CH₃ H CD(CH₃)₂ H CD(CH₃)₂ CD(CH₃)₂ 948. CD₂CH₃ H CD₂CD(CD₃)₂ H CD(CH₃)₂ CD(CH₃)₂ 949. CD₂CH₃ H CD₂CH(CH₃)₂ H CD(CH₃)₂ CD(CH₃)₂ 950. CD₂CH₃ H CD₂C(CD₃)₃ H CD(CH₃)₂ CD(CH₃)₂ 951. CD₂CH₃ H CD₂C(CH₃)₃ H CD(CH₃)₂ CD(CH₃)₂ 952. CD₂CH₃ H CD₂CD₂CF₃ H CD(CH₃)₂ CD(CH₃)₂ 953. CD₂CH₃ H CD₂CH₂CF₃ H CD(CH₃)₂ CD(CH₃)₂ 954. CD₂CH₃ H CD₂CCF₃(CH₃)₂ H CD(CH₃)₂ CD(CH₃)₂ 955. CD₂CH₃ H

H CD(CH₃)₂ CD(CH₃)₂ 956. CD₂CH₃ H

H CD(CH₃)₂ CD(CH₃)₂ 957. CD₂CH₃ H

H CD(CH₃)₂ CD(CH₃)₂ 958. CD₂CH₃ H

H CD(CH₃)₂ CD(CH₃)₂ 959. CD₂CH₃ H

H CD(CH₃)₂ CD(CH₃)₂ 960. CD₂CH₃ H

H CD(CH₃)₂ CD(CH₃)₂ 961. CD₂CH₃ H

H CD(CH₃)₂ CD(CH₃)₂ 962. CD₂CH₃ H

H CD(CH₃)₂ CD(CH₃)₂ 963. CD₂CH₃ H

H CD(CH₃)₂ CD(CH₃)₂ 964. CD₂CH₃ H

H CD(CH₃)₂ CD(CH₃)₂ 965. CD₂CH₃ H

H CD(CH₃)₂ CD(CH₃)₂ 966. CD₂CH₃ H

H CD(CH₃)₂ CD(CH₃)₂ 967. CD₂CH₃ H

H CD(CH₃)₂ CD(CH₃)₂ 968. CD₂CH₃ H

H CD(CH₃)₂ CD(CH₃)₂ 969. CD₂CH₃ H

H CD(CH₃)₂ CD(CH₃)₂ 970. CD₂CH₃ H

H CD(CH₃)₂ CD(CH₃)₂ 971. CD₂CH₃ H

H CD(CH₃)₂ CD(CH₃)₂ 972. CD₂CH₃ H

H CD(CH₃)₂ CD(CH₃)₂ 973. CD₂CH₃ H

H CD(CH₃)₂ CD(CH₃)₂ 974. CD₂CH₃ H

H CD(CH₃)₂ CD(CH₃)₂ 975. CD₂CD₃ CD₃ CD₃ H H CD₂CD(CD₃)₂ 976. CD₂CD₃ CD₃ CD₂CH₃ H H CD₂CD(CD₃)₂ 977. CD₂CD₃ CD₃ CD₂CH₃ H H CD₂CD(CD₃)₂ 978. CD₂CD₃ CD₃ CD(CD₃)₂ H H CD₂CD(CD₃)₂ 979. CD₂CD₃ CD₃ CD(CH₃)₂ H H CD₂CD(CD₃)₂ 980. CD₂CD₃ CD₃ CD₂CD(CD₃)₂ H H CD₂CD(CD₃)₂ 981. CD₂CD₃ CD₃ CD₂CH(CH₃)₂ H H CD₂CD(CD₃)₂ 982. CD₂CH₃ CD₃ CD₂C(CD₃)₃ H H CD₂CD(CD₃)₂ 983. CD₂CD₃ CD₃ CD₂C(CH₃)₃ H H CD₂CD(CD₃)₂ 984. CD₂CD₃ CD₃ CD₂CD₂CF₃ H H CD₂CD(CD₃)₂ 985. CD₂CD₃ CD₃ CD₂CH₂CF₃ H H CD₂CD(CD₃)₂ 986. CD₂CD₃ CD₃ CD₂CCF₃(CH₃)₂ H H CD₂CD(CD₃)₂ 987. CD₂CD₃ CD₃

H H CD₂CD(CD₃)₂ 988. CD₂CD₃ CD₃

H H CD₂CD(CD₃)₂ 989. CD₂CD₃ CD₃

H H CD₂CD(CD₃)₂ 990. CD₂CD₃ CD₃

H H CD₂CD(CD₃)₂ 991. CD₂CD₃ CD₃

H H CD₂CD(CD₃)₂ 992. CD₂CD₃ CD₃

H H CD₂CD(CD₃)₂ 993. CD₂CD₃ CD₃

H H CD₂CD(CD₃)₂ 994. CD₂CD₃ CD₃

H H CD₂CD(CD₃)₂ 995. CD₂CD₃ CD₃

H H CD₂CD(CD₃)₂ 996. CD₂CD₃ CD₃

H H CD₂CD(CD₃)₂ 997. CD₂CD₃ CD₃

H H CD₂CD(CD₃)₂ 998. CD₂CD₃ CD₃

H H CD₂CD(CD₃)₂ 999. CD₂CD₃ CD₃

H H CD₂CD(CD₃)₂ 1000. CD₂CD₃ CD₃

H H CD₂CD(CD₃)₂ 1001. CD₂CD₃ CD₃

H H CD₂CD(CD₃)₂ 1002. CD₂CD₃ CD₃

H H CD₂CD(CD₃)₂ 1003. CD₂CD₃ CD₃

H H CD₂CD(CD₃)₂ 1004. CD₂CD₃ CD₃

H H CD₂CD(CD₃)₂ 1005. CD₂CD₃ CD₃

H H CD₂CD(CD₃)₂ 1006. CD₂CD₃ CD₃

H H CD₂CD(CD₃)₂ 1007. CD₂CH₃ H H CD₃ CD₂CH₃ CD₂CH₃ 1008. CD₂CH₃ H H CD₂CD₃ CD₂CH₃ CD₂CH₃ 1009. CD₂CH₃ H H CD₂CH₃ CD₂CH₃ CD₂CH₃ 1010. CD₂CH₃ H H CD(CD₃)₂ CD₂CH₃ CD₂CH₃ 1011. CD₂CH₃ H H CD(CH₃)₂ CD₂CH₃ CD₂CH₃ 1012. CD₂CH₃ H H CD₂CD(CD₃)₂ CD₂CH₃ CD₂CH₃ 1013. CD₂CH₃ H H CD₂CH(CH₃)₂ CD₂CH₃ CD₂CH₃ 1014. CD₂CH₃ H H CD₂C(CD₃)₃ CD₂CH₃ CD₂CH₃ 1015. CD₂CH₃ H H CD₂C(CH₃)₃ CD₂CH₃ CD₂CH₃ 1016. CD₂CH₃ H H CD₂CD₂CF₃ CD₂CH₃ CD₂CH₃ 1017. CD₂CH₃ H H CD₂CH₂CF₃ CD₂CH₃ CD₂CH₃ 1018. CD₂CH₃ H H CD₂CCF₃(CH₃)₂ CD₂CH₃ CD₂CH₃ 1019. CD₂CH₃ H H

CD₂CH₃ CD₂CH₃ 1020. CD₂CH₃ H H

CD₂CH₃ CD₂CH₃ 1021. CD₂CH₃ H H

CD₂CH₃ CD₂CH₃ 1022. CD₂CH₃ H H

CD₂CH₃ CD₂CH₃ 1023. CD₂CH₃ H H

CD₂CH₃ CD₂CH₃ 1024. CD₂CH₃ H H

CD₂CH₃ CD₂CH₃ 1025. CD₂CH₃ H H

CD₂CH₃ CD₂CH₃ 1026. CD₂CH₃ H H

CD₂CH₃ CD₂CH₃ 1027. CD₂CH₃ H H

CD₂CH₃ CD₂CH₃ 1028. CD₂CH₃ H H

CD₂CH₃ CD₂CH₃ 1029. CD₂CH₃ H H

CD₂CH₃ CD₂CH₃ 1030. CD₂CH₃ H H

CD₂CH₃ CD₂CH₃ 1031. CD₂CH₃ H H

CD₂CH₃ CD₂CH₃ 1032. CD₂CH₃ H H

CD₂CH₃ CD₂CH₃ 1033. CD₂CH₃ H H

CD₂CH₃ CD₂CH₃ 1034. CD₂CH₃ H H

CD₂CH₃ CD₂CH₃ 1035. CD₂CH₃ CD₃ H CD₃ CD(CH₃)₂ CD(CH₃)₂ 1036. CD₂CH₃ CD₃ H CD₂CD₃ CD(CH₃)₂ CD(CH₃)₂ 1037. CD₂CH₃ CD₃ H CD₂CH₃ CD(CH₃)₂ CD(CH₃)₂ 1038. CD₂CH₃ CD₃ H CD(CD₃)₂ CD(CH₃)₂ CD(CH₃)₂ 1039. CD₂CH₃ CD₃ H CD(CH₃)₂ CD(CH₃)₂ CD(CH₃)₂ 1040. CD₂CH₃ CD₃ H CD₂CD(CD₃)₂ CD(CH₃)₂ CD(CH₃)₂ 1041. CD₂CH₃ CD₃ H CD₂CH(CH₃)₂ CD(CH₃)₂ CD(CH₃)₂ 1042. CD₂CH₃ CD₃ H CD₂C(CD₃)₂ CD(CH₃)₂ CD(CH₃)₂ 1043. CD₂CH₃ CD₃ H CD₂C(CH₃)₂ CD(CH₃)₂ CD(CH₃)₂ 1044. CD₂CH₃ CD₃ H CD₂CD₂CF₃ CD(CH₃)₂ CD(CH₃)₂ 1045. CD₂CH₃ CD₃ H CD₂CH₂CF₃ CD(CH₃)₂ CD(CH₃)₂ 1046. CD₂CH₃ CD₃ H CD₂CCF₃(CH₃)₂ CD(CH₃)₂ CD(CH₃)₂ 1047. CD₂CH₃ CD₃ H

CD(CH₃)₂ CD(CH₃)₂ 1048. CD₂CH₃ CD₃ H

CD(CH₃)₂ CD(CH₃)₂ 1049. CD₂CH₃ CD₃ H

CD(CH₃)₂ CD(CH₃)₂ 1050. CD₂CH₃ CD₃ H

CD(CH₃)₂ CD(CH₃)₂ 1051. CD₂CH₃ CD₃ H

CD(CH₃)₂ CD(CH₃)₂ 1052. CD₂CH₃ CD₃ H

CD(CH₃)₂ CD(CH₃)₂ 1053. CD₂CH₃ CD₃ H

CD(CH₃)₂ CD(CH₃)₂ 1054. CD₂CH₃ CD₃ H

CD(CH₃)₂ CD(CH₃)₂ 1055. CD₂CH₃ CD₃ H

CD(CH₃)₂ CD(CH₃)₂ 1056. CD₂CH₃ CD₃ H

CD(CH₃)₂ CD(CH₃)₂ 1057. CD₂CH₃ CD₃ H

CD(CH₃)₂ CD(CH₃)₂ 1058. CD₂CH₃ CD₃ H

CD(CH₃)₂ CD(CH₃)₂ 1059. CD₂CH₃ CD₃ H

CD(CH₃)₂ CD(CH₃)₂ 1060. CD₂CH₃ CD₃ H

CD(CH₃)₂ CD(CH₃)₂ 1061. CD₂CH₃ CD₃ H

CD(CH₃)₂ CD(CH₃)₂ 1062. CD₂CH₃ CD₃ H

CD(CH₃)₂ CD(CH₃)₂ 1063. CD₂CH₃ CD₃ H

CD(CH₃)₂ CD(CH₃)₂ 1064. CD₂CH₃ CD₃ H

CD(CH₃)₂ CD(CH₃)₂ 1065. CD₂CH₃ CD₃ H

CD(CH₃)₂ CD(CH₃)₂ 1066. CD₂CH₃ CD₃ H

CD(CH₃)₂ CD(CH₃)₂ 1067. CD(CH₃)₂ CD₃ H H H

1068. CD(CH₃)₂ CD₂CD₃ H H H

1069. CD(CH₃)₂ CD₂CH₃ H H H

1070. CD(CH₃)₂ CD(CD₃)₂ H H H

1071. CD(CH₃)₂ CD(CH₃)₂ H H H

1072. CD(CH₃)₂ CD₂CD(CD₃)₂ H H H

1073. CD(CH₃)₂ CD₂CH(CH₃)₂ H H H

1074. CD(CH₃)₂ CD₂C(CD₃)₃ H H H

1075. CD(CH₃)₂ CD₂C(CH₃)₃ H H H

1076. CD(CH₃)₂ CD₂CD₂CF₃ H H H

1077. CD(CH₃)₂ CD₂CH₂CF₃ H H H

1078. CD(CH₃)₂ CD₂CCF₃(CH₃)₂ H H H

1079. CD(CH₃)₂

H H H

1080. CD(CH₃)₂

H H H

1081. CD(CH₃)₂

H H H

1082. CD(CH₃)₂

H H H

1083. CD(CH₃)₂

H H H

1084. CD(CH₃)₂

H H H

1085. CD(CH₃)₂

H H H

1086. CD(CH₃)₂

H H H

1087. CD(CH₃)₂

H H H

1088. CD(CH₃)₂

H H H

1089. CD(CH₃)₂

H H H

1090. CD(CH₃)₂

H H H

1091. CD(CH₃)₂

H H H

1092. CD(CH₃)₂

H H H

1093. CD(CH₃)₂

H H H

1094. CD(CH₃)₂

H H H

1095. CD(CH₃)₂

H H H

1096. CD(CH₃)₂

H H H

1097. CD(CH₃)₂

H H H

1098. CD(CH₃)₂

H H H

1099. CD(CD₃)₂ CD₃ H H H

1100. CD(CD₃)₂ CD₂CD₃ H H H

1101. CD(CD₃)₂ CD₂CH₃ H H H

1102. CD(CD₃)₂ CD(CD₃)₂ H H H

1103. CD(CD₃)₂ CD(CH₃)₂ H H H

1104. CD(CD₃)₂ CD₂CD(CD₃)₂ H H H

1105. CD(CD₃)₂ CD₂CH(CH₃)₂ H H H

1106. CD(CD₃)₂ CD₂C(CD₃)₃ H H H

1107. CD(CD₃)₂ CD₂C(CH₃)₃ H H H

1108. CD(CD₃)₂ CD₂CD₂CF₃ H H H

1109. CD(CD₃)₂ CD₂CH₂CF₃ H H H

1110. CD(CD₃)₂ CD₂CCF₃(CH₃)₂ H H H

1111. CD(CD₃)₂

H H H

1112. CD(CD₃)₂

H H H

1113. CD(CD₃)₂

H H H

1114. CD(CD₃)₂

H H H

1115. CD(CD₃)₂

H H H

1116. CD(CD₃)₂

H H H

1117. CD(CD₃)₂

H H H

1118. CD(CD₃)₂

H H H

1119. CD(CD₃)₂

H H H

1120. CD(CD₃)₂

H H H

1121. CD(CD₃)₂

H H H

1122. CD(CD₃)₂

H H H

1123. CD(CD₃)₂

H H H

1124. CD(CD₃)₂

H H H

1125. CD(CD₃)₂

H H H

1126. CD(CD₃)₂

H H H

1127. CD(CD₃)₂

H H H

1128. CD(CD₃)₂

H H H

1129. CD(CD₃)₂

H H H

1130. CD(CD₃)₂

H H H

1131. CH(CH₃)₂ H CH₂CH₃ H H

1132. CH(CH₃)₂ H CH(CH₃)₂ H H

1133. CH(CH₃)₂ H CH₂CH(CH₃)₂ H H

1134. CH(CH₃)₂ H C(CH₃)₃ H H

1135. CH(CH₃)₂ H CH₂C(CH₃)₃ H H

1136. CH(CH₃)₂ H CH₂CH₂CF₃ H H

1137. CH(CH₃)₂ H CH₂CCF₃(CH₃)₂ H H

1138. CH(CH₃)₂ H

H H

1139. CH(CH₃)₂ H

H H

1140. CH(CH₃)₂ H

H H

1141. CH(CH₃)₂ H

H H

1142. CH(CH₃)₂ H

H H

1143. CH(CH₃)₂ H

H H

1144. CH(CH₃)₂ H

H H

1145. CH(CH₃)₂ H

H H

1146. CH(CH₃)₂ H

H H

1147. CH(CH₃)₂ H

H H

1148. CH(CH₃)₂ H

H H

1149. CH(CH₃)₂ H

H H

1150. CH(CH₃)₂ H

H H

1151. CH(CH₃)₂ H

H H

1152. CH(CH₃)₂ H

H H

1153. CH(CH₃)₂ H

H H

1154. CH(CH₃)₂ H

H H

1155. CH(CH₃)₂ H

H H

1156. CH(CH₃)₂ H

H H

1157. CH(CH₃)₂ H

H H

1158. CD(CH₃)₂ H CD₃ H

CD₃ 1159. CD(CH₃)₂ H CD₂CD₃ H

CD₃ 1160. CD(CH₃)₂ H CD₂CH₃ H

CD₃ 1161. CD(CH₃)₂ H CD(CD₃)₂ H

CD₃ 1162. CD(CH₃)₂ H CD(CH₃)₂ H

CD₃ 1163. CD(CH₃)₂ H CD₂CD(CD₃)₂ H

CD₃ 1164. CD(CH₃)₂ H CD₂CH(CH₃)₂ H

CD₃ 1165. CD(CH₃)₂ H CD₂C(CD₃)₃ H

CD₃ 1166. CD(CH₃)₂ H CD₂C(CH₃)₃ H

CD₃ 1167. CD(CH₃)₂ H CD₂CD₂CF₃ H

CD₃ 1168. CD(CH₃)₂ H CD₂CH₂CF₃ H

CD₃ 1169. CD(CH₃)₂ H CD₂CCF₃(CH₃)₂ H

CD₃ 1170. CD(CH₃)₂ H

H

CD₃ 1171. CD(CH₃)₂ H

H

CD₃ 1172. CD(CH₃)₂ H

H

CD₃ 1173. CD(CH₃)₂ H

H

CD₃ 1174. CD(CH₃)₂ H

H

CD₃ 1175. CD(CH₃)₂ H

H

CD₃ 1176. CD(CH₃)₂ H

H

CD₃ 1177. CD(CH₃)₂ H

H

CD₃ 1178. CD(CH₃)₂ H

H

CD₃ 1179. CD(CH₃)₂ H

H

CD₃ 1180. CD(CH₃)₂ H

H

CD₃ 1181. CD(CH₃)₂ H

H

CD₃ 1182. CD(CH₃)₂ H

H

CD₃ 1183. CD(CH₃)₂ H

H

CD₃ 1184. CD(CH₃)₂ H

H

CD₃ 1185. CD(CH₃)₂ H

H

CD₃ 1186. CD(CH₃)₂ H

H

CD₃ 1187. CD(CH₃)₂ H

H

CD₃ 1188. CD(CH₃)₂ H

H

CD₃ 1189. CD(CH₃)₂ H

H

CD₃ 1190. CD(CD₃)₂ H CD₃ H CD(CD₃)₂ CD(CD₃)₂ 1191. CD(CD₃)₂ H CD₂CD₃ H CD(CD₃)₂ CD(CD₃)₂ 1192. CD(CD₃)₂ H CD₂CH₃ H CD(CD₃)₂ CD(CD₃)₂ 1193. CD(CD₃)₂ H CD(CD₃)₂ H CD(CD₃)₂ CD(CD₃)₂ 1194. CD(CD₃)₂ H CD(CH₃)₂ H CD(CD₃)₂ CD(CD₃)₂ 1195. CD(CD₃)₂ H CD₂CD(CD₃)₂ H CD(CD₃)₂ CD(CD₃)₂ 1196. CD(CD₃)₂ H CD₂CH(CH₃)₂ H CD(CD₃)₂ CD(CD₃)₂ 1197. CD(CD₃)₂ H CD₂C(CD₃)₃ H CD(CD₃)₂ CD(CD₃)₂ 1198. CD(CD₃)₂ H CD₂C(CH₃)₃ H CD(CD₃)₂ CD(CD₃)₂ 1199. CD(CD₃)₂ H CD₂CD₂CF₃ H CD(CD₃)₂ CD(CD₃)₂ 1200. CD(CD₃)₂ H CD₂CH₂CF₃ H CD(CD₃)₂ CD(CD₃)₂ 1201. CD(CD₃)₂ H CD₂CCF₃(CH₃)₂ H CD(CD₃)₂ CD(CD₃)₂ 1202. CD(CD₃)₂ H

H CD(CD₃)₂ CD(CD₃)₂ 1203. CD(CD₃)₂ H

H CD(CD₃)₂ CD(CD₃)₂ 1204. CD(CD₃)₂ H

H CD(CD₃)₂ CD(CD₃)₂ 1205. CD(CD₃)₂ H

H CD(CD₃)₂ CD(CD₃)₂ 1206. CD(CD₃)₂ H

H CD(CD₃)₂ CD(CD₃)₂ 1207. CD(CD₃)₂ H

H CD(CD₃)₂ CD(CD₃)₂ 1208. CD(CD₃)₂ H

H CD(CD₃)₂ CD(CD₃)₂ 1209. CD(CD₃)₂ H

H CD(CD₃)₂ CD(CD₃)₂ 1210. CD(CD₃)₂ H

H CD(CD₃)₂ CD(CD₃)₂ 1211. CD(CD₃)₂ H

H CD(CD₃)₂ CD(CD₃)₂ 1212. CD(CD₃)₂ H

H CD(CD₃)₂ CD(CD₃)₂ 1213. CD(CD₃)₂ H

H CD(CD₃)₂ CD(CD₃)₂ 1214. CD(CD₃)₂ H

H CD(CD₃)₂ CD(CD₃)₂ 1215. CD(CD₃)₂ H

H CD(CD₃)₂ CD(CD₃)₂ 1216. CD(CD₃)₂ H

H CD(CD₃)₂ CD(CD₃)₂ 1217. CD(CD₃)₂ H

H CD(CD₃)₂ CD(CD₃)₂ 1218. CD(CD₃)₂ H

H CD(CD₃)₂ CD(CD₃)₂ 1219. CD(CD₃)₂ H

H CD(CD₃)₂ CD(CD₃)₂ 1220. CD(CD₃)₂ H

H CD(CD₃)₂ CD(CD₃)₂ 1221. CD(CD₃)₂ H

H CD(CD₃)₂ CD(CD₃)₂ 1222. CH(CH₃)₂ H H CH₃ H CH₃ 1223. CH(CH₃)₂ H H CH₂CH₃ H CH₃ 1224. CH(CH₃)₂ H H CH(CH₃)₂ H CH3 1225. CH(CH₃)₂ H H CH₂CH(CH₃)₂ H CH₃ 1226. CH(CH₃)₂ H H C(CH₃)₃ H CH₃ 1227. CH(CH₃)₂ H H CH₂C(CH₃)₃ H CH₃ 1228. CH(CH₃)₂ H H CH₂CH₂CF₃ H CH₃ 1229. CH(CH₃)₂ H H CH₂CCF₃(CH₃)₂ H CH₃ 1230. CH(CH₃)₂ H H

H CH₃ 1231. CH(CH₃)₂ H H

H CH₃ 1232. CH(CH₃)₂ H H

H CH₃ 1233. CH(CH₃)₂ H H

H CH₃ 1234. CH(CH₃)₂ H H

H CH₃ 1235. CH(CH₃)₂ H H

H CH₃ 1236. CH(CH₃)₂ H H

H CH₃ 1237. CH(CH₃)₂ H H

H CH₃ 1238. CH(CH₃)₂ H H

H CH₃ 1239. CH(CH₃)₂ H H

H CH₃ 1240. CH(CH₃)₂ H H

H CH₃ 1241. CH(CH₃)₂ H H

H CH₃ 1242. CH(CH₃)₂ H H

H CH₃ 1243. CH(CH₃)₂ H H

H CH₃ 1244. CH(CH₃)₂ H H

H CH₃ 1245. CH(CH₃)₂ H H

H CH₃ 1246. CH(CH₃)₂ H H

H CH₃ 1247. CH(CH₃)₂ H H

H CH₃ 1248. CH(CH₃)₂ H H

H CH₃ 1249. CH(CH₃)₂ H H

H CH₃ 1250. CH(CH₃)₂ CH₃ CH₃ H CH₃ CH₃ 1251. CH(CH₃)₂ CH₂CH₃ CH₃ H CH₃ CH₃ 1252. CH(CH₃)₂ CH(CH₃)₂ CH₃ H CH₃ CH₃ 1253. CH(CH₃)₂ CH₂CH(CH₃)₂ CH₃ H CH₃ CH₃ 1254. CH(CH₃)₂ C(CH₃)₃ CH₃ H CH₃ CH₃ 1255. CH(CH₃)₂ CH₂C(CH₃)₃ CH₃ H CH₃ CH₃ 1256. CH(CH₃)₂ CH₂CH₂CF₃ CH₃ H CH₃ CH₃ 1257. CH(CH₃)₂ CH₂CCF₃(CH₃)₂ CH₃ H CH₃ CH₃ 1258. CH(CH₃)₂

CH₃ H CH₃ CH₃ 1259. CH(CH₃)₂

CH₃ H CH₃ CH₃ 1260. CH(CH₃)₂

CH₃ H CH₃ CH₃ 1261. CH(CH₃)₂

CH₃ H CH₃ CH₃ 1262. CH(CH₃)₂

CH₃ H CH₃ CH₃ 1263. CH(CH₃)₂

CH₃ H CH₃ CH₃ 1264. CH(CH₃)₂

CH₃ H CH₃ CH₃ 1265. CH(CH₃)₂

CH₃ H CH₃ CH₃ 1266. CH(CH₃)₂

CH₃ H CH₃ CH₃ 1267. CH(CH₃)₂

CH₃ H CH₃ CH₃ 1268. CH(CH₃)₂

CH₃ H CH₃ CH₃ 1269. CH(CH₃)₂

CH₃ H CH₃ CH₃ 1270. CH(CH₃)₂

CH₃ H CH₃ CH₃ 1271. CH(CH₃)₂

CH₃ H CH₃ CH₃ 1272. CH(CH₃)₂

CH₃ H CH₃ CH₃ 1273. CH(CH₃)₂

CH₃ H CH₃ CH₃ 1274. CH(CH₃)₂

CH₃ H CH₃ CH₃ 1275. CH(CH₃)₂

CH₃ H CH₃ CH₃ 1276. CH(CH₃)₂

CH₃ H CH₃ CH₃ 1277. CH(CH₃)₂

CH₃ H CH₃ CH₃ 1278. CD(CH₃)₂ CD₃ CD₃ H CH₃ CH₃ 1279. CD(CH₃)₂ CD₂CD₃ CD₃ H CH₃ CH₃ 1280. CD(CH₃)₂ CD₂CH₃ CD₃ H CH₃ CH₃ 1281. CD(CH₃)₂ CD(CD₃)₂ CD₃ H CH₃ CH₃ 1282. CD(CH₃)₂ CD(CH₃)₂ CD₃ H CH₃ CH₃ 1283. CD(CH₃)₂ CD₂CD(CD₃)₂ CD₃ H CH₃ CH₃ 1284. CD(CH₃)₂ CD₂CH(CH₃)₂ CD₃ H CH₃ CH₃ 1285. CD(CH₃)₂ CD₂C(CD₃)₃ CD₃ H CH₃ CH₃ 1286. CD(CH₃)₂ CD₂C(CH₃)₃ CD₃ H CH₃ CH₃ 1287. CD(CH₃)₂ CD₂CD₂CF₃ CD₃ H CH₃ CH₃ 1288. CD(CH₃)₂ CD₂CH₂CF₃ CD₃ H CH₃ CH₃ 1289. CD(CH₃)₂ CD₂CCF₃(CH₃)₂ CD₃ H CH₃ CH₃ 1290. CD(CH₃)₂

CD₃ H CH₃ CH₃ 1291. CD(CH₃)₂

CD₃ H CH₃ CH₃ 1292. CD(CH₃)₂

CD₃ H CH₃ CH₃ 1293. CD(CH₃)₂

CD₃ H CH₃ CH₃ 1294. CD(CH₃)₂

CD₃ H CH₃ CH₃ 1295. CD(CH₃)₂

CD₃ H CH₃ CH₃ 1296. CD(CH₃)₂

CD₃ H CH₃ CH₃ 1297. CD(CH₃)₂

CD₃ H CH₃ CH₃ 1298. CD(CH₃)₂

CD₃ H CH₃ CH₃ 1299. CD(CH₃)₂

CD₃ H CH₃ CH₃ 1300. CD(CH₃)₂

CD₃ H CH₃ CH₃ 1301. CD(CH₃)₂

CD₃ H CH₃ CH₃ 1302. CD(CH₃)₂

CD₃ H CH₃ CH₃ 1303. CD(CH₃)₂

CD₃ H CH₃ CH₃ 1304. CD(CH₃)₂

CD₃ H CH₃ CH₃ 1305. CD(CH₃)₂

CD₃ H CH₃ CH₃ 1306. CD(CH₃)₂

CD₃ H CH₃ CH₃ 1307. CD(CH₃)₂

CD₃ H CH₃ CH₃ 1308. CD(CH₃)₂

CD₃ H CH₃ CH₃ 1309. CD(CH₃)₂

CD₃ H CH₃ CH₃ 1310. CD(CD₃)₂ CD₂CD₃ CD₃ H CD₂CD₃ CD₂CD₃ 1311. CD(CD₃)₂ CD₂CH₃ CD₃ H CD₂CD₃ CD₂CD₃ 1312. CD(CD₃)₂ CD(CD₃)₂ CD₃ H CD₂CD₃ CD₂CD₃ 1313. CD(CD₃)₂ CD(CH₃)₂ CD₃ H CD₂CD₃ CD₂CD₃ 1314. CD(CD₃)₂ CD₂CD(CD₃)₂ CD₃ H CD₂CD₃ CD₂CD₃ 1315. CD(CD₃)₂ CD₂CH(CH₃)₂ CD₃ H CD₂CD₃ CD₂CD₃ 1316. CD(CD₃)₂ CD₂C(CD₃)₃ CD₃ H CD₂CD₃ CD₂CD₃ 1317. CD(CD₃)₂ CD₂C(CH₃)₃ CD₃ H CD₂CD₃ CD₂CD₃ 1318. CD(CD₃)₂ CD₂CD₂CF₃ CD₃ H CD₂CD₃ CD₂CD₃ 1319. CD(CD₃)₂ CD₂CH₂CF₃ CD₃ H CD₂CD₃ CD₂CD₃ 1320. CD(CD₃)₂ CD₂CCF₃(CH₃)₂ CD₃ H CD₂CD₃ CD₂CD₃ 1321. CD(CD₃)₂

CD₃ H CD₂CD₃ CD₂CD₃ 1322. CD(CD₃)₂

CD₃ H CD₂CD₃ CD₂CD₃ 1323. CD(CD₃)₂

CD₃ H CD₂CD₃ CD₂CD₃ 1324. CD(CD₃)₂

CD₃ H CD₂CD₃ CD₂CD₃ 1325. CD(CD₃)₂

CD₃ H CD₂CD₃ CD₂CD₃ 1326. CD(CD₃)₂

CD₃ H CD₂CD₃ CD₂CD₃ 1327. CD(CD₃)₂

CD₃ H CD₂CD₃ CD₂CD₃ 1328. CD(CD₃)₂

CD₃ H CD₂CD₃ CD₂CD₃ 1329. CD(CD₃)₂

CD₃ H CD₂CD₃ CD₂CD₃ 1330. CD(CD₃)₂

CD₃ H CD₂CD₃ CD₂CD₃ 1331. CD(CD₃)₂

CD₃ H CD₂CD₃ CD₂CD₃ 1332. CD(CD₃)₂

CD₃ H CD₂CD₃ CD₂CD₃ 1333. CD(CD₃)₂

CD₃ H CD₂CD₃ CD₂CD₃ 1334. CD(CD₃)₂

CD₃ H CD₂CD₃ CD₂CD₃ 1335. CD(CD₃)₂

CD₃ H CD₂CD₃ CD₂CD₃ 1336. CD(CD₃)₂

CD₃ H CD₂CD₃ CD₂CD₃ 1337. CD(CD₃)₂

CD₃ H CD₂CD₃ CD₂CD₃ 1338. CD(CD₃)₂

CD₃ H CD₂CD₃ CD₂CD₃ 1339. CD(CD₃)₂

CD₃ H CD₂CD₃ CD₂CD₃ 1340. CD(CD₃)₂

CD₃ H CD₂CD₃ CD₂CD₃ 1341. CH(CH₃)₂ CH₃ CH₂CH₃ H CD₂CD₃ CD₂CD₃ 1342. CH(CH₃)₂ CH₃ CH(CH₃)₂ H CD₂CD₃ CD₂CD₃ 1343. CH(CH₃)₂ CH₃ CH₂CH(CH₃)₂ H CD₂CD₃ CD₂CD₃ 1344. CH(CH₃)₂ CH₃ C(CH₃)₃ H CD₂CD₃ CD₂CD₃ 1345. CH(CH₃)₂ CH₃ CH₂C(CH₃)₃ H CD₂CD₃ CD₂CD₃ 1346. CH(CH₃)₂ CH₃ CH₂CH₂CF₃ H CD₂CD₃ CD₂CD₃ 1347. CH(CH₃)₂ CH₃ CH₂CCF₃(CH₃)₂ H CD₂CD₃ CD₂CD₃ 1348. CH(CH₃)₂ CH₃

H CD₂CD₃ CD₂CD₃ 1349. CH(CH₃)₂ CH₃

H CD₂CD₃ CD₂CD₃ 1350. CH(CH₃)₂ CH₃

H CD₂CD₃ CD₂CD₃ 1351. CH(CH₃)₂ CH₃

H CD₂CD₃ CD₂CD₃ 1352. CH(CH₃)₂ CH₃

H CD₂CD₃ CD₂CD₃ 1353. CH(CH₃)₂ CH₃

H CD₂CD₃ CD₂CD₃ 1354. CH(CH₃)₂ CH₃

H CD₂CD₃ CD₂CD₃ 1355. CH(CH₃)₂ CH₃

H CD₂CD₃ CD₂CD₃ 1356. CH(CH₃)₂ CH₃

H CD₂CD₃ CD₂CD₃ 1357. CH(CH₃)₂ CH₃

H CD₂CD₃ CD₂CD₃ 1358. CH(CH₃)₂ CH₃

H CD₂CD₃ CD₂CD₃ 1359. CH(CH₃)₂ CH₃

H CD₂CD₃ CD₂CD₃ 1360. CH(CH₃)₂ CH₃

H CD₂CD₃ CD₂CD₃ 1361. CH(CH₃)₂ CH₃

H CD₂CD₃ CD₂CD₃ 1362. CH(CH₃)₂ CH₃

H CD₂CD₃ CD₂CD₃ 1363. CH(CH₃)₂ CH₃

H CD₂CD₃ CD₂CD₃ 1364. CH(CH₃)₂ CH₃

H CD₂CD₃ CD₂CD₃ 1365. CH(CH₃)₂ CH₃

H CD₂CD₃ CD₂CD₃ 1366. CH(CH₃)₂ CH₃

H CD₂CD₃ CD₂CD₃ 1367. CH(CH₃)₂ CH₃

H CD₂CD₃ CD₂CD₃ 1368. CD(CH₃)₂ CD₃ CD₂CD₃ H CD₂CD₃ CD₂CD₃ 1369. CD(CH₃)₂ CD₃ CD₂CH₃ H CD₂CD₃ CD₂CD₃ 1370. CD(CH₃)₂ CD₃ CD(CD₃)₂ H CD₂CD₃ CD₂CD₃ 1371. CD(CH₃)₂ CD₃ CD(CH₃)₂ H CD₂CD₃ CD₂CD₃ 1372. CD(CH₃)₂ CD₃ CD₂CD(CD₃)₂ H CD₂CD₃ CD₂CD₃ 1373. CD(CH₃)₂ CD₃ CD₂CH(CH₃)₂ H CD₂CD₃ CD₂CD₃ 1374. CD(CH₃)₂ CD₃ CD₂C(CD₃)₃ H CD₂CD₃ CD₂CD₃ 1375. CD(CH₃)₂ CD₃ CD₂C(CH₃)₃ H CD₂CD₃ CD₂CD₃ 1376. CD(CH₃)₂ CD₃ CD₂CD₂CF₃ H CD₂CD₃ CD₂CD₃ 1377. CD(CH₃)₂ CD₃ CD₂CH₂CF₃ H CD₂CD₃ CD₂CD₃ 1378. CD(CH₃)₂ CD₃ CD₂CCF₃(CH₃)₂ H CD₂CD₃ CD₂CD₃ 1379. CD(CH₃)₂ CD₃

H CD₂CD₃ CD₂CD₃ 1380. CD(CH₃)₂ CD₃

H CD₂CD₃ CD₂CD₃ 1381. CD(CH₃)₂ CD₃

H CD₂CD₃ CD₂CD₃ 1382. CD(CH₃)₂ CD₃

H CD₂CD₃ CD₂CD₃ 1383. CD(CH₃)₂ CD₃

H CD₂CD₃ CD₂CD₃ 1384. CD(CH₃)₂ CD₃

H CD₂CD₃ CD₂CD₃ 1385. CD(CH₃)₂ CD₃

H CD₂CD₃ CD₂CD₃ 1386. CD(CH₃)₂ CD₃

H CD₂CD₃ CD₂CD₃ 1387. CD(CH₃)₂ CD₃

H CD₂CD₃ CD₂CD₃ 1388. CD(CH₃)₂ CD₃

H CD₂CD₃ CD₂CD₃ 1389. CD(CH₃)₂ CD₃

H CD₂CD₃ CD₂CD₃ 1390. CD(CH₃)₂ CD₃

H CD₂CD₃ CD₂CD₃ 1391. CD(CH₃)₂ CD₃

H CD₂CD₃ CD₂CD₃ 1392. CD(CH₃)₂ CD₃

H CD₂CD₃ CD₂CD₃ 1393. CD(CH₃)₂ CD₃

H CD₂CD₃ CD₂CD₃ 1394. CD(CH₃)₂ CD₃

H CD₂CD₃ CD₂CD₃ 1395. CD(CH₃)₂ CD₃

H CD₂CD₃ CD₂CD₃ 1396. CD(CH₃)₂ CD₃

H CD₂CD₃ CD₂CD₃ 1397. CD(CH₃)₂ CD₃

H CD₂CD₃ CD₂CD₃ 1398. CD(CH₃)₂ CD₃

H CD₂CD₃ CD₂CD₃ 1399.

CD₃ H H H CD₃ 1400.

CD₃ CD₃ H H CD₃ 1401.

CD₃ H CD₃ H CD₃ 1402.

CD₃ CD₃ CD₃ H CD₃ 1403.

CD₃ H H H CD₃ 1404.

CD₃ CD₃ H H CD₃ 1405.

CD₃ H CD₃ H CD₃ 1406.

CD₃ CD₃ CD₃ H CD₃ 1407.

CD₃ H H H CD₃ 1408.

CD₃ CD₃ H H CD₃ 1409.

CD₃ H CD₃ H CD₃ 1410.

CD₃ CD₃ CD₃ H CD₃ 1411.

CD₃ H H H CD₃ 1412.

CD₃ CD₃ H H CD₃ 1413.

CD₃ H CD₃ H CD₃ 1414.

CD₃ CD₃ CD₃ H CD₃ 1415.

CD₃ H H H CD₃ 1416.

CD₃ CD₃ H H CD₃ 1417.

CD₃ H CD₃ H CD₃ 1418.

CD₃ CD₃ CD₃ H CD₃ 1419.

CD₃ H H H CD₃ 1420.

CD₃ CD₃ H H CD₃ 1421.

CD₃ H CD₃ H CD₃ 1422.

CD₃ CD₃ CD₃ H CD₃ 1423.

CD₃ H H H CD₃ 1424.

CD₃ CD₃ H H CD₃ 1425.

CD₃ H CD₃ H CD₃ 1426.

CD₃ CD₃ CD₃ H CD₃ 1427.

CD₃ H H H CD₃ 1428.

CD₃ CD₃ H H CD₃ 1429.

CD₃ H CD₃ H H 1430.

CD₃ CD₃ CD₃ H H 1431. CD₃ H

H H H 1432. CD₃ CD₃ CD₃ H H H

In some embodiments, the compound has a formula of ML_(n)(L_(B))_(m-n), where M is Ir or Pt; L_(B) is a bidentate ligand; when M is Ir, m is 3, and n is 1, 2, or 3; and when M is Pt, m is 2, and n is 1, or 2.

In some such embodiments, the compound has a formula of IrL₃. In some such embodiments, the compound has a formula of IrL(L_(B))₂; and wherein L_(B) is different from L.

In some embodiments, the compound has a formula of Ir(L)₂(L_(B)), and L_(B) is different from L.

In some embodiments, the compound has a formula of Pt(L)(L_(B)), and wherein L and L_(B) can be the same or different. In some such embodiments, L and L_(B) are connected to form a tetradentate ligand. In some embodiments, wherein L and L_(B) are connected at two places to form a macrocyclic tetradentate ligand.

In some embodiments where the compound has a formula of ML_(n)(L_(B))_(m-n), either (i) M is Ir, m is 3, and n is 1 or 2, or (ii) M is Pt, m is 2, and n is 1; and L_(B) is selected from the group consisting of:

where:

-   -   each of X¹ to X¹³ are independently selected from the group         consisting of carbon and nitrogen;     -   X is selected from the group consisting of BR′, NR′, PR′, O, S,         Se, C═O, S═O, SO₂, CR′R″, SiR′R″, and GeR′R″;     -   R′ and R″ are optionally fused or joined to form a ring;     -   each R_(a), R_(b), R_(c), and R_(d) may represent from mono         substitution to the possible maximum number of substitution, or         no substitution;     -   R′, R″, R_(a), R_(b), R_(c), and R_(d) are each independently         selected from the group consisting of hydrogen, deuterium,         halide, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy,         aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl,         alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acids,         ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl,         phosphino, and combinations thereof; and     -   any two adjacent substitutents of R_(a), R_(b), R_(c), and R_(d)         are optionally fused or joined to form a ring or form a         multidentate ligand.

In some embodiments where the compound has a formula of ML_(n)(L_(B))_(m-n), either (i) M is Ir, m is 3, and n is 1 or 2, or (ii) M is Pt, m is 2, and n is 1; and L_(B) is selected from the group consisting of L_(B1) to L_(B300) as shown below:

Ligand L can be L^(A1) to L^(A1432), L^(B1) to L^(B1432), L^(C1) to L^(C1432), and L^(D1) to L^(D1432), while L_(B) can be another ligand in the organometallic complex. Thus, it should be readily apparent that ligands L^(B1) to L^(B1432) are different and distinct from ligands L_(B1) to L_(B300).

In some embodiments, the compound is selected from the group consisting of compound A-1 to compound A-429,600, compound B-1 to compound B-429,600, compound C-1 to compound C-429,600, and compound D-1 to compound D-429,600, where:

-   -   Compound k-x has the formula Ir(L^(ki))(L_(Bj))₂;     -   x=300i+j−300; k is A, B, C, or D; i is an integer from 1 to         1430, and j is an integer from 1 to 300; and     -   L_(B1) to L_(B300) have the structures provided herein.

In some embodiments, the compound can be an emissive dopant. In some embodiments, the compound can produce emissions via phosphorescence, fluorescence, thermally activated delayed fluorescence, i.e., TADF (also referred to as E-type delayed fluorescence), triplet-triplet annihilation, or combinations of these processes.

In another embodiment, an organic light emitting device (OLED) comprising an anode; a cathode; and an organic layer, disposed between the anode and the cathode is described. In some embodiments, a consumer product containing an OLED as described herein is described. The organic layer includes a compound having a ligand L having the formula:

as described herein.

According to another aspect of the present disclosure, a formulation comprising the compound having a ligand L with the structure

is provided.

The OLED disclosed herein can be incorporated into one or more of a consumer product, an electronic component module, and a lighting panel. The organic layer can be an emissive layer and the compound can be an emissive dopant in some embodiments, while the compound can be a non-emissive dopant in other embodiments.

The organic layer can also include a host. In some embodiments, two or more hosts are preferred. In some embodiments, the hosts used maybe a) bipolar, b) electron transporting, c) hole transporting or d) wide band gap materials that play little role in charge transport. In some embodiments, the host can include a metal complex. The host can be a triphenylene containing benzo-fused thiophene or benzo-fused furan. Any substituent in the host can be an unfused substituent independently selected from the group consisting of C_(n)H_(2n+1), OC_(n)H_(2n+1), OAr₁, N(C_(n)H_(2n+1))₂, N(Ar₁)(Ar₂), CH═CH—C_(n)H_(2n+1), C≡C—C_(n)H_(2n+1), Ar₁, Ar₁-Ar₂, and C_(n)H_(2n)-Ar₁, or the host has no substitutions. In the preceding substituents n can range from 1 to 10; and Ar₁ and Ar₂ can be independently selected from the group consisting of benzene, biphenyl, naphthalene, triphenylene, carbazole, and heteroaromatic analogs thereof. The host can be an inorganic compound. For example, a Zn containing inorganic material e.g. ZnS.

The host can be a compound comprising at least one chemical group selected from the group consisting of triphenylene, carbazole, dibenzothiophene, dibenzofuran, dibenzoselenophene, azatriphenylene, azacarbazole, aza-dibenzothiophene, aza-dibenzofuran, and aza-dibenzoselenophene. The host can include a metal complex. The host can be, but is not limited to, a specific compound selected from the group consisting of:

and combinations thereof. Additional information on possible hosts is provided below.

In yet another aspect of the present disclosure, a formulation that comprises a compound according to Formula I is described. The formulation can include one or more components selected from the group consisting of a solvent, a host, a hole injection material, hole transport material, and an electron transport layer material, disclosed herein.

Combination with Other Materials

The materials described herein as useful for a particular layer in an organic light emitting device may be used in combination with a wide variety of other materials present in the device. For example, emissive dopants disclosed herein may be used in conjunction with a wide variety of hosts, transport layers, blocking layers, injection layers, electrodes and other layers that may be present. The materials described or referred to below are non-limiting examples of materials that may be useful in combination with the compounds disclosed herein, and one of skill in the art can readily consult the literature to identify other materials that may be useful in combination.

Conductivity Dopants:

A charge transport layer can be doped with conductivity dopants to substantially alter its density of charge carriers, which will in turn alter its conductivity. The conductivity is increased by generating charge carriers in the matrix material, and depending on the type of dopant, a change in the Fermi level of the semiconductor may also be achieved. Hole-transporting layer can be doped by p-type conductivity dopants and n-type conductivity dopants are used in the electron-transporting layer.

Non-limiting examples of the conductivity dopants that may be used in an OLED in combination with materials disclosed herein are exemplified below together with references that disclose those materials: EP01617493, EP01968131, EP2020694, EP2684932, US20050139810, US20070160905, US20090167167, US2010288362, WO06081780, WO2009003455, WO2009008277, WO2009011327, WO2014009310, US2007252140, US2015060804 and US2012146012.

HIL/HTL:

A hole injecting/transporting material to be used in the present invention is not particularly limited, and any compound may be used as long as the compound is typically used as a hole injecting/transporting material. Examples of the material include, but are not limited to: a phthalocyanine or porphyrin derivative; an aromatic amine derivative; an indolocarbazole derivative; a polymer containing fluorohydrocarbon; a polymer with conductivity dopants; a conducting polymer, such as PEDOT/PSS; a self-assembly monomer derived from compounds such as phosphonic acid and silane derivatives; a metal oxide derivative, such as MoO_(x); a p-type semiconducting organic compound, such as 1,4,5,8,9,12-Hexaazatriphenylenehexacarbonitrile; a metal complex, and a cross-linkable compounds.

Examples of aromatic amine derivatives used in HIL or HTL include, but not limit to the following general structures:

Each of Ar¹ to Ar⁹ is selected from the group consisting of aromatic hydrocarbon cyclic compounds such as benzene, biphenyl, triphenyl, triphenylene, naphthalene, anthracene, phenalene, phenanthrene, fluorene, pyrene, chrysene, perylene, and azulene; the group consisting of aromatic heterocyclic compounds such as dibenzothiophene, dibenzofuran, dibenzoselenophene, furan, thiophene, benzofuran, benzothiophene, benzoselenophene, carbazole, indolocarbazole, pyridylindole, pyrrolodipyridine, pyrazole, imidazole, triazole, oxazole, thiazole, oxadiazole, oxatriazole, dioxazole, thiadiazole, pyridine, pyridazine, pyrimidine, pyrazine, triazine, oxazine, oxathiazine, oxadiazine, indole, benzimidazole, indazole, indoxazine, benzoxazole, benzisoxazole, benzothiazole, quinoline, isoquinoline, cinnoline, quinazoline, quinoxaline, naphthyridine, phthalazine, pteridine, xanthene, acridine, phenazine, phenothiazine, phenoxazine, benzofuropyridine, furodipyridine, benzothienopyridine, thienodipyridine, benzoselenophenopyridine, and selenophenodipyridine; and the group consisting of 2 to 10 cyclic structural units which are groups of the same type or different types selected from the aromatic hydrocarbon cyclic group and the aromatic heterocyclic group and are bonded to each other directly or via at least one of oxygen atom, nitrogen atom, sulfur atom, silicon atom, phosphorus atom, boron atom, chain structural unit and the aliphatic cyclic group. Each Ar may be unsubstituted or may be substituted by a substituent selected from the group consisting of deuterium, halide, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acids, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof.

In one aspect, Ar¹ to Ar⁹ is independently selected from the group consisting of:

wherein k is an integer from 1 to 20; X¹⁰¹ to X¹⁰⁸ is C (including CH) or N; Z¹⁰¹ is NAr¹, O, or S; Ar¹ has the same group defined above.

Examples of metal complexes used in HIL or HTL include, but are not limited to the following general formula:

wherein Met is a metal, which can have an atomic weight greater than 40; (Y¹⁰¹-Y¹⁰²) is a bidentate ligand, Y¹⁰¹ and Y¹⁰² are independently selected from C, N, O, P, and S; L¹⁰¹ is an ancillary ligand; k′ is an integer value from 1 to the maximum number of ligands that may be attached to the metal; and k′+k″ is the maximum number of ligands that may be attached to the metal.

In one aspect, (Y¹⁰¹-Y¹⁰²) is a s a 2-phenylpyridine derivative. In another aspect, (Y¹⁰¹-Y¹⁰²) is a carbene ligand. In another aspect, Met is selected from Ir, Pt, Os, and Zn. In a further aspect, the metal complex has a smallest oxidation potential in solution vs. Fc⁺/Fc couple less than about 0.6 V.

Non-limiting examples of the HIL and HTL materials that may be used in an OLED in combination with materials disclosed herein are exemplified below together with references that disclose those materials: CN102702075, DE102012005215, EP01624500, EP01698613, EP01806334, EP01930964, EP01972613, EP01997799, EP02011790, EP02055700, EP02055701, EP1725079, EP2085382, EP2660300, EP650955, JP07-073529, JP2005112765, JP2007091719, JP2008021687, JP2014-009196, KR20110088898, KR20130077473, TW201139402, U.S. Ser. No. 06/517,957, US20020158242, US20030162053, US20050123751, US20060182993, US20060240279, US20070145888, US20070181874, US20070278938, US20080014464, US20080091025, US20080106190, US20080124572, US20080145707, US20080220265, US20080233434, US20080303417, US2008107919, US20090115320, US20090167161, US2009066235, US2011007385, US20110163302, US2011240968, US2011278551, US2012205642, US2013241401, US20140117329, US2014183517, U.S. Pat. No. 5,061,569, U.S. Pat. No. 5,639,914, WO05075451, WO07125714, WO08023550, WO08023759, WO2009145016, WO2010061824, WO2011075644, WO2012177006, WO2013018530, WO2013039073, WO2013087142, WO2013118812, WO2013120577, WO2013157367, WO2013175747, WO2014002873, WO2014015935, WO2014015937, WO2014030872, WO2014030921, WO2014034791, WO2014104514, WO2014157018.

EBL:

An electron blocking layer (EBL) may be used to reduce the number of electrons and/or excitons that leave the emissive layer. The presence of such a blocking layer in a device may result in substantially higher efficiencies, and or longer lifetime, as compared to a similar device lacking a blocking layer. Also, a blocking layer may be used to confine emission to a desired region of an OLED. In some embodiments, the EBL material has a higher LUMO (closer to the vacuum level) and/or higher triplet energy than the emitter closest to the EBL interface. In some embodiments, the EBL material has a higher LUMO (closer to the vacuum level) and or higher triplet energy than one or more of the hosts closest to the EBL interface. In one aspect, the compound used in EBL contains the same molecule or the same functional groups used as one of the hosts described below.

Host:

The light emitting layer of the organic EL device of the present invention preferably contains at least a metal complex as light emitting material, and may contain a host material using the metal complex as a dopant material. Examples of the host material are not particularly limited, and any metal complexes or organic compounds may be used as long as the triplet energy of the host is larger than that of the dopant. Any host material may be used with any dopant so long as the triplet criteria is satisfied.

Examples of metal complexes used as host are preferred to have the following general formula:

wherein Met is a metal; (Y¹⁰³-Y¹⁰⁴) is a bidentate ligand, Y¹⁰³ and Y¹⁰⁴ are independently selected from C, N, O, P, and S; L¹⁰¹ is an another ligand; k′ is an integer value from 1 to the maximum number of ligands that may be attached to the metal; and k′+k″ is the maximum number of ligands that may be attached to the metal.

In one aspect, the metal complexes are:

wherein (O—N) is a bidentate ligand, having metal coordinated to atoms O and N.

In another aspect, Met is selected from Ir and Pt. In a further aspect, (Y¹⁰³-Y¹⁰⁴) is a carbene ligand.

Examples of other organic compounds used as host are selected from the group consisting of aromatic hydrocarbon cyclic compounds such as benzene, biphenyl, triphenyl, triphenylene, tetraphenylene, naphthalene, anthracene, phenalene, phenanthrene, fluorene, pyrene, chrysene, perylene, and azulene; the group consisting of aromatic heterocyclic compounds such as dibenzothiophene, dibenzofuran, dibenzoselenophene, furan, thiophene, benzofuran, benzothiophene, benzoselenophene, carbazole, indolocarbazole, pyridylindole, pyrrolodipyridine, pyrazole, imidazole, triazole, oxazole, thiazole, oxadiazole, oxatriazole, dioxazole, thiadiazole, pyridine, pyridazine, pyrimidine, pyrazine, triazine, oxazine, oxathiazine, oxadiazine, indole, benzimidazole, indazole, indoxazine, benzoxazole, benzisoxazole, benzothiazole, quinoline, isoquinoline, cinnoline, quinazoline, quinoxaline, naphthyridine, phthalazine, pteridine, xanthene, acridine, phenazine, phenothiazine, phenoxazine, benzofuropyridine, furodipyridine, benzothienopyridine, thienodipyridine, benzoselenophenopyridine, and selenophenodipyridine; and the group consisting of 2 to 10 cyclic structural units which are groups of the same type or different types selected from the aromatic hydrocarbon cyclic group and the aromatic heterocyclic group and are bonded to each other directly or via at least one of oxygen atom, nitrogen atom, sulfur atom, silicon atom, phosphorus atom, boron atom, chain structural unit and the aliphatic cyclic group. Each option within each group may be unsubstituted or may be substituted by a substituent selected from the group consisting of deuterium, halide, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acids, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof.

In one aspect, the host compound contains at least one of the following groups in the molecule:

wherein each of R¹⁰¹ to R¹⁰⁷ is independently selected from the group consisting of hydrogen, deuterium, halide, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acids, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof, and when it is aryl or heteroaryl, it has the similar definition as Ar's mentioned above. k is an integer from 0 to 20 or 1 to 20; k′″ is an integer from 0 to 20. X¹⁰¹ to X¹⁰⁸ is selected from C (including CH) or N. Z¹⁰¹ and Z¹⁰² is selected from NR¹⁰¹, O, or S.

Non-limiting examples of the host materials that may be used in an OLED in combination with materials disclosed herein are exemplified below together with references that disclose those materials: EP2034538, EP2034538A, EP2757608, JP2007254297, KR20100079458, KR20120088644, KR20120129733, KR20130115564, TW201329200, US20030175553, US20050238919, US20060280965, US20090017330, US20090030202, US20090167162, US20090302743, US20090309488, US20100012931, US20100084966, US20100187984, US2010187984, US2012075273, US2012126221, US2013009543, US2013105787, US2013175519, US2014001446, US20140183503, US20140225088, US2014034914, U.S. Pat. No. 7,154,114, WO2001039234, WO2004093207, WO2005014551, WO2005089025, WO2006072002, WO2006114966, WO2007063754, WO2008056746, WO2009003898, WO2009021126, WO2009063833, WO2009066778, WO2009066779, WO2009086028, WO2010056066, WO2010107244, WO2011081423, WO2011081431, WO2011086863, WO2012128298, WO2012133644, WO2012133649, WO2013024872, WO2013035275, WO2013081315, WO2013191404, WO2014142472,

Additional Emitters:

One or more additional emitter dopants may be used in conjunction with the compound of the present disclosure. Examples of the additional emitter dopants are not particularly limited, and any compounds may be used as long as the compounds are typically used as emitter materials. Examples of suitable emitter materials include, but are not limited to, compounds which can produce emissions via phosphorescence, fluorescence, thermally activated delayed fluorescence, i.e., TADF (also referred to as E-type delayed fluorescence), triplet annihilation, or combinations of these processes.

Non-limiting examples of the emitter materials that may be used in an OLED in combination with materials disclosed herein are exemplified below together with references that disclose those materials: CN103694277, CN1696137, EB01238981, EP01239526, EP01961743, EP1239526, EP1244155, EP1642951, EP1647554, EP1841834, EP1841834B, EP2062907, EP2730583, JP2012074444, JP2013110263, JP4478555, KR1020090133652, KR20120032054, KR20130043460, TW201332980, U.S. Ser. No. 06/699,599, U.S. Ser. No. 06/916,554, US20010019782, US20020034656, US20030068526, US20030072964, US20030138657, US20050123788, US20050244673, US2005123791, US2005260449, US20060008670, US20060065890, US20060127696, US20060134459, US20060134462, US20060202194, US20060251923, US20070034863, US20070087321, US20070103060, US20070111026, US20070190359, US20070231600, US2007034863, US2007104979, US2007104980, US2007138437, US2007224450, US2007278936, US20080020237, US20080233410, US20080261076, US20080297033, US200805851, US2008161567, US2008210930, US20090039776, US20090108737, US20090115322, US20090179555, US2009085476, US2009104472, US20100090591, US20100148663, US20100244004, US20100295032, US2010102716, US2010105902, US2010244004, US2010270916, US20110057559, US20110108822, US20110204333, US2011215710, US2011227049, US2011285275, US2012292601, US20130146848, US2013033172, US2013165653, US2013181190, US2013334521, US20140246656, US2014103305, U.S. Pat. No. 6,303,238, U.S. Pat. No. 6,413,656, U.S. Pat. No. 6,653,654, U.S. Pat. No. 6,670,645, U.S. Pat. No. 6,687,266, U.S. Pat. No. 6,835,469, U.S. Pat. No. 6,921,915, U.S. Pat. No. 7,279,704, U.S. Pat. No. 7,332,232, U.S. Pat. No. 7,378,162, U.S. Pat. No. 7,534,505, U.S. Pat. No. 7,675,228, U.S. Pat. No. 7,728,137, U.S. Pat. No. 7,740,957, U.S. Pat. No. 7,759,489, U.S. Pat. No. 7,951,947, U.S. Pat. No. 8,067,099, U.S. Pat. No. 8,592,586, U.S. Pat. No. 8,871,361, WO06081973, WO06121811, WO07018067, WO07108362, WO07115970, WO07115981, WO08035571, WO2002015645, WO2003040257, WO2005019373, WO2006056418, WO2008054584, WO2008078800, WO2008096609, WO2008101842, WO2009000673, WO2009050281, WO2009100991, WO2010028151, WO2010054731, WO2010086089, WO2010118029, WO2011044988, WO2011051404, WO2011107491, WO2012020327, WO2012163471, WO2013094620, WO2013107487, WO2013174471, WO2014007565, WO2014008982, WO2014023377, WO2014024131, WO2014031977, WO2014038456, WO2014112450.

HBL:

A hole blocking layer (HBL) may be used to reduce the number of holes and/or excitons that leave the emissive layer. The presence of such a blocking layer in a device may result in substantially higher efficiencies and/or longer lifetime as compared to a similar device lacking a blocking layer. Also, a blocking layer may be used to confine emission to a desired region of an OLED. In some embodiments, the HBL material has a lower HOMO (further from the vacuum level) and or higher triplet energy than the emitter closest to the HBL interface. In some embodiments, the HBL material has a lower HOMO (further from the vacuum level) and or higher triplet energy than one or more of the hosts closest to the HBL interface.

In one aspect, compound used in HBL contains the same molecule or the same functional groups used as host described above.

In another aspect, compound used in HBL contains at least one of the following groups in the molecule:

wherein k is an integer from 1 to 20; L¹⁰¹ is an another ligand, k′ is an integer from 1 to 3.

ETL:

Electron transport layer (ETL) may include a material capable of transporting electrons. Electron transport layer may be intrinsic (undoped), or doped. Doping may be used to enhance conductivity. Examples of the ETL material are not particularly limited, and any metal complexes or organic compounds may be used as long as they are typically used to transport electrons.

In one aspect, compound used in ETL contains at least one of the following groups in the molecule:

wherein R¹⁰¹ is selected from the group consisting of hydrogen, deuterium, halide, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acids, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof, when it is aryl or heteroaryl, it has the similar definition as Ar's mentioned above. Ar¹ to Ar³ has the similar definition as Ar's mentioned above. k is an integer from 1 to 20. X¹⁰¹ to X¹⁰⁸ is selected from C (including CH) or N.

In another aspect, the metal complexes used in ETL contains, but not limit to the following general formula:

wherein (O—N) or (N—N) is a bidentate ligand, having metal coordinated to atoms O, N or N, N; L¹⁰¹ is another ligand; k′ is an integer value from 1 to the maximum number of ligands that may be attached to the metal.

Non-limiting examples of the ETL materials that may be used in an OLED in combination with materials disclosed herein are exemplified below together with references that disclose those materials: CN103508940, EP01602648, EP01734038, EP01956007, JP2004-022334, JP2005149918, JP2005-268199, KR0117693, KR20130108183, US20040036077, US20070104977, US2007018155, US20090101870, US20090115316, US20090140637, US20090179554, US2009218940, US2010108990, US2011156017, US2011210320, US2012193612, US2012214993, US2014014925, US2014014927, US20140284580, U.S. Pat. No. 6,656,612, U.S. Pat. No. 8,415,031, WO2003060956, WO2007111263, WO2009148269, WO2010067894, WO2010072300, WO2011074770, WO2011105373, WO2013079217, WO2013145667, WO2013180376, WO2014104499, WO2014104535,

Charge Generation Layer (CGL)

In tandem or stacked OLEDs, the CGL plays an essential role in the performance, which is composed of an n-doped layer and a p-doped layer for injection of electrons and holes, respectively. Electrons and holes are supplied from the CGL and electrodes. The consumed electrons and holes in the CGL are refilled by the electrons and holes injected from the cathode and anode, respectively; then, the bipolar currents reach a steady state gradually. Typical CGL materials include n and p conductivity dopants used in the transport layers.

In any above-mentioned compounds used in each layer of the OLED device, the hydrogen atoms can be partially or fully deuterated. Thus, any specifically listed substituent, such as, without limitation, methyl, phenyl, pyridyl, etc. may be undeuterated, partially deuterated, and fully deuterated versions thereof. Similarly, classes of substituents such as, without limitation, alkyl, aryl, cycloalkyl, heteroaryl, etc. also may be undeuterated, partially deuterated, and fully deuterated versions thereof.

Experimental Synthesis of compound Ir L^(A1431)(L_(B91))₂

Step 1

A 250 mL two-necked round-bottomed flask was flushed with nitrogen, then charged with 2-bromo-4-chloro-5-methylpyridine (9.88 g, 47.9 mmol), phenylboronic acid (6.42 g, 52.6 mmol), diacetoxypalladium (0.537 g, 2.393 mmol), triphenylphosphane (2.51 g, 9.57 mmol), potassium hydroxide (5.37 g, 96 mmol) and acetonitrile (150 ml)/ethanol (75 ml) mixture under nitrogen to give a red suspension. The reaction mixture was heated to 60° C. under nitrogen for 16 hrs. Then the reaction mixture was cooled to room temperature (˜22° C.), filtered through a silica gel pad, and evaporated to dryness. The residue was purified by column chromatography (silica gel, heptanes/EtOAc=2/1 (v:v)) and crystallized from heptanes as colorless crystals (6.5 g, 67% yield).

Step 2

4-Chloro-5-methyl-2-phenylpyridine (5 g, 24.55 mmol), (4-cyclohexylphenyl)boronic acid (5.01 g, 24.55 mmol), potassium phosphate tribasic monohydrate (11.31 g, 49.1 mmol), tris(dibenzylideneacetone)dipalladium(0) (Pd₂(dba)₃) (2 mol %) and 2-dicyclohexylphosphino-2′,6′-dimethoxybiphenyl (SPhos) (4 mol %) were dissolved in a dimethoxyethane (DME) (70 ml)/water (5 ml) mixture under nitrogen to give a red suspension. The reaction mixture was degassed and heated to reflux for 16 hrs.

The reaction mixture was then cooled to room temperature (˜22° C.). The organic phase was then separated, filtered, evaporated, and purified by column chromatography on silica gel, eluted with heptanes/tetrahydrofuran (THF) 9/1 (v/v) to yield a clear solidified colorless oil (6.8 g, 85% yield).

Step 3

4-(4-Cyclohexylphenyl)-5-methyl-2-phenylpyridine (6.8 g, 20.77 mmol), ((methyl-d₃)sulfinyl)methane-d₃ (61.2 g, 727 mmol), and sodium 2-methylpropan-2-olate (0.998 g, 10.38 mmol) were suspended together in a flask under nitrogen. The flask was immersed in an oil bath at 71° C. for 18 hrs. The reaction mixture was then cooled to room temperature (˜22° C.), quenched with 3 equivalents of D₂O, diluted with brine, and extracted with EtOAc. The organic phase was separated, filtered, evaporated, and purified using a silica gel column, eluted with heptanes/THF 95/5 (v/v) to yield colorless crystals (6.0 g, 87% yield).

Step 4

Methanol-solvated iridium triflate salt (4 g, 5.12 mmol) and 4-(4-(cyclohexyl-1-d)phenyl)-5-(methyl-d₃)-2-phenylpyridine (5.94 g, 17.90 mmol) were suspended in an ethanol (30 ml)/methanol (30.0 ml) mixture under nitrogen. The reaction mixture was degassed, then the flask was immersed in the oil bath at 70° C. for 3 days. The reaction mixture then was cooled to room temperature (˜22° C.) and filtered, and the solid material was dried. The mixture was purified by column chromatographyon silica gel column that was eluted with a gradient heptane/toluene 4/1 to 1/4 (v/v) mixture. Pure fractions were evaporated and crystallized from DCM/ethanol, to produce 1.8 g (39% yield) of bright yellow solid.

Synthesis of Ir L^(A1432)(L_(B91))₂

Step 1

4-Chloro-5-methyl-2-phenylpyridine (6 g, 29.5 mmol), (3,4-dimethylphenyl)boronic acid (4.86 g, 32.4 mmol), and potassium phosphate tribasic hydrate (13.57 g, 58.9 mmol) were dissolved in a mixture of DME (60 ml)/water (2 mL) under nitrogen to give a colorless suspension. Pd₂(dba)₃ (0.405 g, 0.442 mmol) and SPhos (0.410 g, 0.884 mmol) were added as one portion, before the reaction mixture was degassed and heated to 100° C. under nitrogen for 16 h. The reaction mixture was then cooled down to room temperature (˜22° C.). The organic phase was separated, evaporated, and purified by column chromatography using a silica gel column eluted with heptanes/THF 95/5 (v/v), then crystallized from heptanes to yield white crystals (7.0 g, 85% yield).

Step 2

4-(3,4-Dimethylphenyl)-5-methyl-2-phenylpyridine (7 g, 25.6 mmol), ((methyl-d3)sulfinyl)methane-d3 (86 g, 1024 mmol), and sodium 2-methylpropan-2-olate (1.723 g, 17.92 mmol) were mixed in a flask under nitrogen to give a brown solution. The flask was immersed in an oil bath at 71° C. for 14 h, cooled down to room temperature (˜22° C.), quenched with 3 equivalents of D₂O, then diluted with brine. The resulting solution was extracted with EtOAc and the organic extracts were combined, filtered and evaporated. The crude material was purified by column chromatography using a silica gel column eluted with heptanes/THF 95/5 (v/v) to yield 4-(3,4-bis(methyl-d3)phenyl)-5-(methyl-d3)-2-phenylpyridine as a white solid (6.0 g, 83% yield).

Step 3

Methanol-solvated iridium triflate salt (2.8 g, 3.58 mmol) and 4-(3,4-bis(methyl-d3)phenyl)-5-(methyl-d3)-2-phenylpyridine (3.03 g, 10.74 mmol) were suspended in an EtOH (30 ml)/MeOH (30.0 ml) mixture in a flask under nitrogen to give a yellow suspension. The flask was immersed in the oil bath 71° C. and stirred under nitrogen for 3 days. The resulting mixture was cooled to room temperature (˜22° C.) and the resulting yellow solid was filtered off and purified by column chromatography using a silica gel column eluted with toluene/heptanes 85/15 (v/v), then crystallized from toluene/ethanol and toluene/heptanes to yield a yellow solid (1.8 g, 59% yield). Device Examples

All example devices were fabricated by high vacuum (<10⁻⁷ Torr) thermal evaporation. The anode electrode was 800 Å of indium tin oxide (ITO). The cathode consisted of 10 Å of Liq (8-hydroxyquinoline lithium) followed by 1,000 Å of Al. All devices were encapsulated with a glass lid sealed with an epoxy resin in a nitrogen glove box (<1 ppm of H₂O and O₂) immediately after fabrication with a moisture getter incorporated inside the package. The organic stack of the device examples consisted of sequentially, from the ITO Surface: 100 Å of HAT-CN as the hole injection layer (HIL); 450 Å of HTM as a hole transporting layer (HTL); emissive layer (EML) with thickness 400 Å. Emissive layer containing H-host (HO: E-host (H2) in 6:4 ratio and 12 weight % of green emitter. 350 Å of Liq (8-hydroxyquinoline lithium) doped with 40% of ETM as the ETL. Table 1 shows the schematic device structure. The chemical structures of the device materials are shown below.

The fabricated devices were evaluated for EL, JVL and lifetime at DC 80 mA/cm². LT97 at 9,000 nits was calculated from 80 mA/cm2 LT data assuming an acceleration factor of 1.8. Device performance is shown in the table 2.

TABLE 1 schematic device structure Layer Material Thickness [Å] Anode ITO 800 HIL HAT-CN 100 HTL HTM 450 Green H1:H2: example 400 EML dopant ETL Liq:ETM 40% 350 EIL Liq 10 Cathode Al 1,000

TABLE 2 Device performance 1931 CIE At 10 mA/cm² At 9K nits λ max FWHM Voltage LE EQE PE Calculated Emitter 12% x y [nm] [nm] [V] [cd/A] [%] [lm/W] 97%[h]** Comparative Example 0.373 0.598 539 80 4.7 81.8 22.5 54.8 1,084 Ir L^(A1431)(L_(B91))₂ 0.365 0.603 537 78 4.6 92.2 25.2 62.3 1,194 Ir L^(A1432)(L_(B91))₂ 0.347 0.613 532 77 4.5 86.5 23.6 59.8 1,194

The efficiency of example Ir L^(A1431)(L_(B91))₂ and Ir L^(A1432)(L_(B91))₂ is higher than the comparative example. Presumably, the alike substitution in the peripheral ring has better alignment with transition dipolar moment of the molecular. The concept is illustrated in the following image. Furthermore, compounds Ir L^(A1431)(L_(B91))₂ and Ir L^(A1432)(L_(B91))₂ are both blue shifted from the comparative example with a lower device lifetime.

It is understood that the various embodiments described herein are by way of example only, and are not intended to limit the scope of the invention. For example, many of the materials and structures described herein may be substituted with other materials and structures without deviating from the spirit of the invention. The present invention as claimed may therefore include variations from the particular examples and preferred embodiments described herein, as will be apparent to one of skill in the art. It is understood that various theories as to why the invention works are not intended to be limiting. 

1. A compound comprising a ligand L having the formula:

wherein R¹ and R⁶ represents mono, di, tri, or tetra substitution, or no substitution; wherein R² represents mono, di, or tri substitution, or no substitution; wherein each R¹, R², R³, R⁴, R⁴, R⁵, R⁶, R⁷, and R⁸ is independently selected from the group consisting of hydrogen, deuterium, halide, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acids, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof; wherein any adjacent substituents of R¹ R², R³, R⁴, R⁵, R⁶, R⁷, and R⁸ are optionally joined or fused into a ring; wherein at least one of R³, R⁴, and R⁵ is not hydrogen; wherein a is an integer from 0 to 10; wherein (i) when a is 0, at least one of R⁷, R⁸, and an R² adjacent to ring B, is not hydrogen, and (ii) when a is 1 to 10, at least one of an R² adjacent to ring A and an R⁶ adjacent to ring C is not hydrogen; wherein the ligand L is coordinated to a metal M having an atomic weight greater than 40; and wherein the ligand L is optionally linked with other ligands to comprise a tridentate, tetradentate, pentadentate or hexadentate ligand.
 2. The compound of claim 1, wherein M is selected from the group consisting of Ir, Rh, Re, Ru, Os, Pt, Au, and Cu.
 3. The compound of claim 1, wherein M is Ir or Pt.
 4. (canceled)
 5. (canceled)
 6. The compound of claim 1, wherein (i) when a is 0, at least one of R⁷, R⁸, and an R² adjacent to ring B, is selected from the group consisting of alkyl, cycloalkyl, partially or fully deuterated variants thereof, and combinations thereof, and (ii) when a is 1 to 10, at least one of an R² adjacent to ring A and an R⁶ adjacent to ring C is selected from the group consisting of alkyl, cycloalkyl, partially or fully deuterated variants thereof, and combinations thereof.
 7. The compound of claim 1, wherein at least one of R³, R⁴, and R⁵ is selected from the group consisting of alkyl, cycloalkyl, fluorine, partially or fully deuterated variants thereof, and combinations thereof.
 8. (canceled)
 9. The compound of claim 1, wherein (i) when a is 0, at least one R² adjacent to ring B is not hydrogen, and at least one of R⁷, and R⁸ is not hydrogen, and (ii) when a is 1 to 10, at least at one R² adjacent to ring A is not hydrogen, and at least one R⁶ adjacent to ring C is not hydrogen.
 10. (canceled)
 11. The compound of claim 1, wherein ligand L is selected from the group consisting of:


12. The compound of claim 1, wherein ligand L is selected from the group consisting of L^(A1) to L^(A1432), L^(B1) to L^(B1432), L^(C1) to L^(C1432), L^(D1) to L^(D1432) as defined in the following table based on the structures of


1. i in L^(Ai), L^(Bi),
 6. R⁷
 7. R⁸ or L^(Ci), L^(Di)
 2. R²
 3. R³
 4. R⁴
 5. R⁵ or R⁶¹ R⁶²
 1. 8. CH₃
 9. H
 10. CH₃
 11. H
 12. H
 13. CH₃
 2. 14. CH₃
 15. H
 16. CH₂CH₃
 17. H
 18. H
 19. CH₃
 3. 20. CH₃
 21. H
 22. CH(CH₃)₂
 23. H
 24. H
 25. CH₃
 4. 26. CH₃
 27. H
 28. CH₂CH(CH₃)₂
 29. H
 30. H
 31. CH₃
 5. 32. CH₃
 33. H
 34. C(CH₃)₃
 35. H
 36. H
 37. CH₃
 6. 38. CH₃
 39. H
 40. CH₂C(CH₃)₃
 41. H
 42. H
 43. CH₃
 7. 44. CH₃
 45. H
 46. CH₂CH₂CF₃
 47. H
 48. H
 49. CH₃
 8. 50. CH₃
 51. H
 52. CH₂CCF₃(CH₃)₂
 53. H
 54. H
 55. CH₃
 9. 56. CH₃
 57. H
 58.


59. H
 60. H
 61. CH₃
 10. 62. CH₃
 63. H
 64.


65. H
 66. H
 67. CH₃
 11. 68. CH₃
 69. H
 70.


71. H
 72. H
 73. CH₃
 12. 74. CH₃
 75. H
 76.


77. H
 78. H
 79. CH₃
 13. 80. CH₃
 81. H
 82.


83. H
 84. H
 85. CH₃
 14. 86. CH₃
 87. H 88 .


89. H
 90. H
 91. CH₃
 15. 92. CH₃
 93. H
 94.


95. H
 96. H
 97. CH₃
 16. 98. CH₃
 99. H
 100.


101. H
 102. H
 103. CH₃
 17. 104. CH₃
 105. H
 106.


107. H
 108. H
 109. CH₃
 18. 110. CH₃
 111. H
 112.


113. H
 114. H
 115. CH₃
 19. 116. CH₃
 117. H
 118.


119. H
 120. H
 121. CH₃
 20. 122. CH₃
 123. H
 124.


125. H
 126. H
 127. CH₃
 21. 128. CH₃
 129. H
 130.


131. H
 132. H
 133. CH₃
 22. 134. CH₃
 135. H
 136.


137. H
 138. H
 139. CH₃
 23. 140. CH₃
 141. H
 142.


143. H
 144. H
 145. CH₃
 24. 146. CH₃
 147. H
 148.


149. H
 150. H
 151. CH₃
 25. 152. CH₃
 153. H
 154.


155. H
 156. H
 157. CH₃
 26. 158. CH₃
 159. H
 160.


161. H
 162. H
 163. CH₃
 27. 164. CH₃
 165. H
 166. CH₃
 167. H
 168. CH₃
 169. CH₃
 28. 170. CH₃
 171. H
 172. CH₂CH₃
 173. H
 174. CH₃
 175. CH₃
 29. 176. CH₃
 177. H
 178. CH(CH₃)₂
 179. H
 180. CH₃
 181. CH₃
 30. 182. CH₃
 183. H
 184. CH₂CH(CH₃)₂
 185. H
 186. CH₃
 187. CH₃
 31. 188. CH₃
 189. H
 190. C(CH₃)₃
 191. H
 192. CH₃
 193. CH₃
 32. 194. CH₃
 195. H
 196. CH₂C(CH₃)₃
 197. H
 198. CH₃
 199. CH₃
 33. 200. CH₃
 201. H
 202. CH₂C H₂CF₃
 203. H
 204. CH₃
 205. CH₃
 34. 206. CH₃
 207. H
 208. CH₂CCF₃(CH₃)₂
 209. H
 210. CH₃
 211. CH₃
 35. 212. CH₃
 213. H
 214.


215. H
 216. CH₃
 217. CH₃
 36. 218. CH₃
 219. H
 220.


221. H
 222. CH₃
 223. CH₃
 37. 224. CH₃
 225. H
 226.


227. H
 228. CH₃
 229. CH₃
 38. 230. CH₃
 231. H
 232.


233. H
 234. CH₃
 235. CH₃
 39. 236. CH₃
 237. H
 238.


239. H
 240. CH₃
 241. CH₃
 40. 242. CH₃
 243. H
 244.


245. H
 246. CH₃
 247. CH₃
 41. 248. CH₃
 249. H
 250.


251. H
 252. CH₃
 253. CH₃
 42. 254. CH₃
 255. H
 256.


257. H
 258. CH₃
 259. CH₃
 43. 260. CH₃
 261. H
 262.


263. H
 264. CH₃
 265. CH₃
 44. 266. CH₃
 267. H
 268.


269. H
 270. CH₃
 271. CH₃
 45. 272. CH₃
 273. H
 274.


275. H
 276. CH₃
 277. CH₃
 46. 278. CH₃
 279. H
 280.


281. H
 282. CH₃
 283. CH₃
 47. 284. CH₃
 285. H
 286.


287. H
 288. CH₃
 289. CH₃
 48. 290. CH₃
 291. H
 292.


293. H
 294. CH₃
 295. CH₃
 49. 296. CH₃
 297. H
 298.


299. H
 300. CH₃
 301. CH₃
 50. 302. CH₃
 303. H
 304.


305. H
 306. CH₃
 307. CH₃
 51. 308. CH₃
 309. H
 310.


311. H
 312. CH₃
 313. CH₃
 52. 314. CH₃
 315. H
 316.


317. H
 318. CH₃
 319. CH₃
 53. 320. H
 321. H
 322. CH₃
 323. H
 324. H
 325. CH₃
 54. 326. H
 327. H
 328. CH₂CH₃
 329. H
 330. H
 331. CH₃
 55. 332. H
 333. H
 334. CH(CH₃)₂
 335. H
 336. H
 337. CH₃
 56. 338. H
 339. H
 340. CH₂CH(CH₃)₂
 341. H
 342. H
 343. CH₃
 57. 344. H
 345. H
 346. C(CH₃)₃
 347. H
 348. H
 349. CH₃
 58. 350. H
 351. H
 352. CH₂C(CH₃)₃
 353. H
 354. H
 355. CH₃
 59. 356. H
 357. H
 358. CH₂CH₂CF₃
 359. H
 360. H
 361. CH₃
 60. 362. H
 363. H
 364. CH₂CCF₃(CH₃)₂
 365. H
 366. H
 367. CH₃
 61. 368. H
 369. H
 370.


371. H
 372. H
 373. CH₃
 62. 374. H
 375. H
 376.


377. H
 378. H
 379. CH₃
 63. 380. H
 381. H
 382.


383. H
 384. H
 385. CH₃
 64. 386. H
 387. H
 388.


389. H
 390. H
 391. CH₃
 65. 392. H
 393. H
 394.


395. H
 396. H
 397. CH₃
 66. 398. H
 399. H
 400.


401. H
 402. H
 403. CH₃
 67. 404. H
 405. H
 406.


407. H
 408. H
 409. CH₃
 68. 410. H
 411. H
 412.


413. H
 414. H
 415. CH₃
 69. 416. H
 417. H
 418.


419. H
 420. H
 421. CH₃
 70. 422. H
 423. H
 424.


425. H
 426. H
 427. CH₃
 71. 428. H
 429. H 430 .


431. H
 432. H
 433. CH₃
 72. 434. H
 435. H
 436.


437. H
 438. H
 439. CH₃
 73. 440. H
 441. H
 442.


443. H
 444. H
 445. CH₃
 74. 446. H
 447. H
 448.


449. H
 450. H
 451. CH₃
 75. 452. H
 453. H
 454.


455. H
 456. H
 457. CH₃
 76. 458. H
 459. H
 460.


461. H
 462. H
 463. CH₃
 77. 464. H
 465. H
 466.


467. H
 468. H
 469. CH₃
 78. 470. H
 471. H
 472.


473. H
 474. H
 475. CH₃
 79. 476. H
 477. H
 478. CH₃
 479. H
 480. CH₃
 481. CH₃
 80. 482. H
 483. H
 484. CH₂CH₃
 485. H
 486. CH₃
 487. CH₃
 81. 488. H
 489. H
 490. CH(CH₃)₂
 491. H
 492. CH₃
 493. CH₃
 82. 494. H
 495. H
 496. CH₂CH(CH₃)₂
 497. H
 498. CH₃
 499. CH₃
 83. 500. H
 501. H
 502. C(CH₃)₃
 503. H
 504. CH₃
 505. CH₃
 84. 506. H
 507. H
 508. CH₂C(CH₃)₃
 509. H
 510. CH₃
 511. CH₃
 85. 512. H
 513. H
 514. CH₂CH₂CF₃
 515. H
 516. CH₃
 517. CH₃
 86. 518. H
 519. H
 520. CH₂CCF₃(CH₃)₂
 521. H
 522. CH₃
 523. CH₃
 87. 524. H
 525. H
 526.


527. H
 528. CH₃
 529. CH₃
 88. 530. H
 531. H
 532.


533. H
 534. CH₃
 535. CH₃
 89. 536. H
 537. H
 538.


539. H
 540. CH₃
 541. CH₃
 90. 542. H
 543. H
 544.


545. H
 546. CH₃
 547. CH₃
 91. 548. H
 549. H
 550.


551. H
 552. CH₃
 553. CH₃
 92. 554. H
 555. H 556 .


557. H
 558. CH₃
 559. CH₃
 93. 560. H
 561. H
 562.


563. H
 564. CH₃
 565. CH₃
 94. 566. H
 567. H
 568.


569. H
 570. CH₃
 571. CH₃
 95. 572. H
 573. H
 574.


575. H
 576. CH₃
 577. CH₃
 96. 578. H
 579. H
 580.


581. H
 582. CH₃
 583. CH₃
 97. 584. H
 585. H
 586.


587. H
 588. CH₃
 589. CH₃
 98. 590. H
 591. H
 592.


593. H
 594. CH₃
 595. CH₃
 99. 596. H
 597. H
 598.


599. H
 600. CH₃
 601. CH₃
 100. 602. H
 603. H
 604.


605. H
 606. CH₃
 607. CH₃
 101. 608. H
 609. H
 610.


611. H
 612. CH₃
 613. CH₃
 102. 614. H
 615. H
 616.


617. H
 618. CH₃
 619. CH₃
 103. 620. H
 621. H
 622.


623. H
 624. CH₃
 625. CH₃
 104. 626. H
 627. H
 628.


629. H
 630. CH₃
 631. CH₃
 105. 632. CH₃
 633. H
 634. CH₃
 635. CH₃
 636. H
 637. CH₃
 106. 638. CH₃
 639. H
 640. CH₂CH₃
 641. CH₃
 642. H
 643. CH₃
 107. 644. CH₃
 645. H
 646. CH(CH₃)₂
 647. CH₃
 648. H
 649. CH₃
 108. 650. CH₃
 651. H
 652. CH₂CH(CH₃)₂
 653. CH₃
 654. H
 655. CH₃
 109. 656. CH₃
 657. H
 658. C(CH₃)₃
 659. CH₃
 660. H
 661. CH₃
 110. 662. CH₃
 663. H
 664. CH₂C(CH₃)₃
 665. CH₃
 666. H
 667. CH₃
 111. 668. CH₃
 669. H
 670. CH₂CH₂CF₃
 671. CH₃
 672. H
 673. CH₃
 112. 674. CH₃
 675. H
 676. CH₂CCF₃(CH₃)₂
 677. CH₃
 678. H
 679. CH₃
 113. 680. CH₃
 681. H
 682.


683. CH₃
 684. H
 685. CH₃
 114. 686. CH₃
 687. H
 688.


689. CH₃
 690. H
 691. CH₃
 115. 692. CH₃
 693. H
 694.


695. CH₃
 696. H
 697. CH₃
 116. 698. CH₃
 699. H
 700.


701. CH₃
 702. H
 703. CH₃
 117. 704. CH₃
 705. H
 706.


707. CH₃
 708. H
 709. CH₃
 118. 710. CH₃
 711. H 712 .


713. CH₃
 714. H
 715. CH₃
 119. 716. CH₃
 717. H
 718.


719. CH₃
 720. H
 721. CH₃
 120. 722. CH₃
 723. H
 724.


725. CH₃
 726. H
 727. CH₃
 121. 728. CH₃
 729. H
 730.


731. CH₃
 732. H
 733. CH₃
 122. 734. CH₃
 735. H
 736.


737. CH₃
 738. H
 739. CH₃
 123. 740. CH₃
 741. H
 742.


743. CH₃
 744. H
 745. CH₃
 124. 746. CH₃
 747. H
 748.


749. CH₃
 750. H
 751. CH₃
 125. 752. CH₃
 753. H
 754.


755. CH₃
 756. H
 757. CH₃
 126. 758. CH₃
 759. H
 760.


761. CH₃
 762. H
 763. CH₃
 127. 764. CH₃
 765. H
 766.


767. CH₃
 768. H
 769. CH₃
 128. 770. CH₃
 771. H
 772.


773. CH₃
 774. H
 775. CH₃
 129. 776. CH₃
 777. H
 778.


779. CH₃
 780. H
 781. CH₃
 130. 782. CH₃
 783. H
 784.


785. CH₃
 786. H
 787. CH₃
 131. 788. CH₃
 789. CH₃
 790. CH₃
 791. CH₃
 792. H
 793. CH₃
 132. 794. CH₃
 795. CH₃
 796. CH₂CH₃
 797. CH₃
 798. H
 799. CH₃
 133. 800. CH₃
 801. CH₃
 802. CH(CH₃)₂
 803. CH₃
 804. H
 805. CH₃
 134. 806. CH₃
 807. CH₃
 808. CH₂CH(CH₃)₂
 809. CH₃
 810. H
 811. CH₃
 135. 812. CH₃
 813. CH₃
 814. C(CH₃)₃
 815. CH₃
 816. H
 817. CH₃
 136. 818. CH₃
 819. CH₃
 820. CH₂C(CH₃)₃
 821. CH₃
 822. H
 823. CH₃
 137. 824. CH₃
 825. CH₃
 826. CH₂CH₂CF₃
 827. CH₃
 828. H
 829. CH₃
 138. 830. CH₃
 831. CH₃
 832. CH₂CCF₃(CH₃)₂
 833. CH₃
 834. H
 835. CH₃
 139. 836. CH₃
 837. CH₃
 838.


839. CH₃
 840. H
 841. CH₃
 140. 842. CH₃
 843. CH₃
 844.


845. CH₃
 846. H
 847. CH₃
 141. 848. CH₃
 849. CH₃
 850.


851. CH₃
 852. H
 853. CH₃
 142. 854. CH₃
 855. CH₃
 856.


857. CH₃
 858. H
 859. CH₃
 143. 860. CH₃
 861. CH₃
 862.


863. CH₃
 864. H
 865. CH₃
 144. 866. CH₃
 867. CH₃ 868 .


869. CH₃
 870. H
 871. CH₃
 145. 872. CH₃
 873. CH₃
 874.


875. CH₃
 876. H
 877. CH₃
 146. 878. CH₃
 879. CH₃
 880.


881. CH₃
 882. H
 883. CH₃
 147. 884. CH₃
 885. CH₃
 886.


887. CH₃
 888. H
 889. CH₃
 148. 890. CH₃
 891. CH₃
 892.


893. CH₃
 894. H
 895. CH₃
 149. 896. CH₃
 897. CH₃
 898.


899. CH₃
 900. H
 901. CH₃
 150. 902. CH₃
 903. CH₃
 904.


905. CH₃
 906. H
 907. CH₃
 151. 908. CH₃
 909. CH₃
 910.


911. CH₃
 912. H
 913. CH₃
 152. 914. CH₃
 915. CH₃
 916.


917. CH₃
 918. H
 919. CH₃
 153. 920. CH₃
 921. CH₃
 922.


923. CH₃
 924. H
 925. CH₃
 154. 926. CH₃
 927. CH₃
 928.


929. CH₃
 930. H
 931. CH₃
 155. 932. CH₃
 933. CH₃
 934.


935. CH₃
 936. H
 937. CH₃
 156. 938. CH₃
 939. CH₃
 940.


941. CH₃
 942. H
 943. CH₃
 157. 944. CH₃
 945. CH₃
 946.


947. CH₃
 948. H
 949. CH₃
 158. 950. CH₃
 951. CH₃
 952.


953. CH₃
 954. H
 955. CH₃
 159. 956. CD₃
 957. H
 958. CD₃
 959. H
 960. H
 961. CD₃
 160. 962. CD₃
 963. H
 964. CD₂CD₃
 965. H
 966. H
 967. CD₃
 161. 968. CD₃
 969. H
 970. CD₂CH₃
 971. H
 972. H
 973. CD₃
 162. 974. CD₃
 975. H
 976. CD(CD₃)₂
 977. H
 978. H
 979. CD₃
 163. 980. CD₃
 981. H
 982. CD(CH₃)₂
 983. H
 984. H
 985. CD₃
 164. 986. CD₃
 987. H
 988. CD₂CD(CD₃)₂
 989. H
 990. H
 991. CD₃
 165. 992. CD₃
 993. H
 994. CD₂CH(CH₃)₂
 995. H
 996. H
 997. CD₃
 166. 998. CD₃
 999. H
 1000. CD₂C(CD₃)₃
 1001. H
 1002. H
 1003. CD₃
 167. 1004. CD₃
 1005. H
 1006. CD₂C(CH₃)₃
 1007. H
 1008. H
 1009. CD₃
 168. 1010. CD₃
 1011. H
 1012. CD₂CD₂CF₃
 1013. H
 1014. H
 1015. CD₃
 169. 1016. CD₃
 1017. H
 1018. CD₂CH₂CF₃
 1019. H
 1020. H
 1021. CD₃
 170. 1022. CD₃
 1023. H
 1024. CD₂CCF₃(CH₃)₂
 1025. H
 1026. H
 1027. CD₃
 171. 1028. CD₃
 1029. H
 1030.


1031. H
 1032. H
 1033. CD₃
 172. 1034. CD₃
 1035. H
 1036.


1037. H
 1038. H
 1039. CD₃
 173. 1040. CD₃
 1041. H
 1042.


1043. H
 1044. H
 1045. CD₃
 174. 1046. CD₃
 1047. H
 1048.


1049. H
 1050. H
 1051. CD₃
 175. 1052. CD₃
 1053. H
 1054.


1055. H
 1056. H
 1057. CD₃
 176. 1058. CD₃
 1059. H
 1060.


1061. H
 1062. H
 1063. CD₃
 177. 1064. CD₃
 1065. H
 1066.


1067. H
 1068. H
 1069. CD₃
 178. 1070. CD₃
 1071. H
 1072.


1073. H
 1074. H
 1075. CD₃
 179. 1076. CD₃
 1077. H
 1078.


1079. H
 1080. H
 1081. CD₃
 180. 1082. CD₃
 1083. H
 1084.


1085. H
 1086. H
 1087. CD₃
 181. 1088. CD₃
 1089. H
 1090.


1091. H
 1092. H
 1093. CD₃
 182. 1094. CD₃
 1095. H
 1096.


1097. H
 1098. H
 1099. CD₃
 183. 1100. CD₃
 1101. H
 1102.


1103. H
 1104. H
 1105. CD₃
 184. 1106. CD₃
 1107. H
 1108.


1109. H
 1110. H
 1111. CD₃
 185. 1112. CD₃
 1113. H
 1114.


1115. H
 1116. H
 1117. CD₃
 186. 1118. CD₃
 1119. H
 1120.


1121. H
 1122. H
 1123. CD₃
 187. 1124. CD₃
 1125. H
 1126.


1127. H
 1128. H
 1129. CD₃
 188. 1130. CD₃
 1131. H
 1132.


1133. H
 1134. H
 1135. CD₃
 189. 1136. CD₃
 1137. H
 1138.


1139. H
 1140. H
 1141. CD₃
 190. 1142. CD₃
 1143. H
 1144.


1145. H
 1146. H
 1147. CD₃
 191. 1148. CD₃
 1149. H
 1150. CD₃
 1151. H
 1152. CD₃
 1153. CD₃
 192. 1154. CD₃
 1155. H
 1156. CD₂CD₃
 1157. H
 1158. CD₃
 1159. CD₃
 193. 1160. CD₃
 1161. H
 1162. CD₂CH₃
 1163. H
 1164. CD₃
 1165. CD₃
 194. 1166. CD₃
 1167. H
 1168. CD(CD₃)₂
 1169. H
 1170. CD₃
 1171. CD₃
 195. 1172. CD₃
 1173. H
 1174. CD(CH₃)₂
 1175. H
 1176. CD₃
 1177. CD₃
 196. 1178. CD₃
 1179. H
 1180. CD₂CD(CD₃)₂
 1181. H
 1182. CD₃
 1183. CD₃
 197. 1184. CD₃
 1185. H
 1186. CD₂CH(CH₃)₂
 1187. H
 1188. CD₃
 1189. CD₃
 198. 1190. CD₃
 1191. H
 1192. CD₂C(CD₃)₃
 1193. H
 1194. CD₃
 1195. CD₃
 199. 1196. CD₃
 1197. H
 1198. CD₂C(CH₃)₃
 1199. H
 1200. CD₃
 1201. CD₃
 200. 1202. CD₃
 1203. H
 1204. CD₂CD₂CF₃
 1205. H
 1206. CD₃
 1207. CD₃
 201. 1208. CD₃
 1209. H
 1210. CD₂CH₂CF₃
 1211. H
 1212. CD₃
 1213. CD₃
 202. 1214. CD₃
 1215. H
 1216. CD₂CCF₃(CH₃)₂
 1217. H
 1218. CD₃
 1219. CD₃
 203. 1220. CD₃
 1221. H
 1222.


1223. H
 1224. CD₃
 1225. CD₃
 204. 1226. CD₃
 1227. H
 1228.


1229. H
 1230. CD₃
 1231. CD₃
 205. 1232. CD₃
 1233. H
 1234.


1235. H
 1236. CD₃
 1237. CD₃
 206. 1238. CD₃
 1239. H
 1240.


1241. H
 1242. CD₃
 1243. CD₃
 207. 1244. CD₃
 1245. H
 1246.


1247. H
 1248. CD₃
 1249. CD₃
 208. 1250. CD₃
 1251. H
 1252.


1253. H
 1254. CD₃
 1255. CD₃
 209. 1256. CD₃
 1257. H
 1258.


1259. H
 1260. CD₃
 1261. CD₃
 210. 1262. CD₃
 1263. H
 1264.


1265. H
 1266. CD₃
 1267. CD₃
 211. 1268. CD₃
 1269. H
 1270.


1271. H
 1272. CD₃
 1273. CD₃
 212. 1274. CD₃
 1275. H
 1276.


1277. H
 1278. CD₃
 1279. CD₃
 213. 1280. CD₃
 1281. H
 1282.


1283. H
 1284. CD₃
 1285. CD₃
 214. 1286. CD₃
 1287. H
 1288.


1289. H
 1290. CD₃
 1291. CD₃
 215. 1292. CD₃
 1293. H
 1294.


1295. H
 1296. CD₃
 1297. CD₃
 216. 1298. CD₃
 1299. H
 1300.


1301. H
 1302. CD₃
 1303. CD₃
 217. 1304. CD₃
 1305. H
 1306.


1307. H
 1308. CD₃
 1309. CD₃
 218. 1310. CD₃
 1311. H
 1312.


1313. H
 1314. CD₃
 1315. CD₃
 219. 1316. CD₃
 1317. H
 1318.


1319. H
 1320. CD₃
 1321. CD₃
 220. 1322. CD₃
 1323. H
 1324.


1325. H
 1326. CD₃
 1327. CD₃
 221. 1328. CD₃
 1329. H
 1330.


1331. H
 1332. CD₃
 1333. CD₃
 222. 1334. CD₃
 1335. H
 1336.


1337. H
 1338. CD₃
 1339. CD₃
 223. 1340. H
 1341. H
 1342. CD₃
 1343. H
 1344. H
 1345. CD₃
 224. 1346. H
 1347. H
 1348. CD₂CD₃
 1349. H
 1350. H
 1351. CD₃
 225. 1352. H
 1353. H
 1354. CD₂CH₃
 1355. H
 1356. H
 1357. CD₃
 226. 1358. H
 1359. H
 1360. CD(CD₃)₂
 1361. H
 1362. H
 1363. CD₃
 227. 1364. H
 1365. H
 1366. CD(CH₃)₂
 1367. H
 1368. H
 1369. CD₃
 228. 1370. H
 1371. H
 1372. CD₂CD(CD₃)₂
 1373. H
 1374. H
 1375. CD₃
 229. 1376. H
 1377. H
 1378. CD₂CH(CH₃)₂
 1379. H
 1380. H
 1381. CD₃
 230. 1382. H
 1383. H
 1384. CD₂C(CD₃)₃
 1385. H
 1386. H
 1387. CD₃
 231. 1388. H
 1389. H
 1390. CD₂C(CH₃)₃
 1391. H
 1392. H
 1393. CD₃
 232. 1394. H
 1395. H
 1396. CD₂CD₂CF₃
 1397. H
 1398. H
 1399. CD₃
 233. 1400. H
 1401. H
 1402. CD₂CH₂CF₃
 1403. H
 1404. H
 1405. CD₃
 234. 1406. H
 1407. H
 1408. CD₂CCF₃(CH₃)₂
 1409. H
 1410. H
 1411. CD₃
 235. 1412. H
 1413. H
 1414.


1415. H
 1416. H
 1417. CD₃
 236. 1418. H
 1419. H
 1420.


1421. H
 1422. H
 1423. CD₃
 237. 1424. H
 1425. H
 1426.


1427. H
 1428. H
 1429. CD₃
 238. 1430. H
 1431. H
 1432.


1433. H
 1434. H
 1435. CD₃
 239. 1436. H
 1437. H
 1438.


1439. H
 1440. H
 1441. CD₃
 240. 1442. H
 1443. H
 1444.


1445. H
 1446. H
 1447. CD₃
 241. 1448. H
 1449. H
 1450.


1451. H
 1452. H
 1453. CD₃
 242. 1454. H
 1455. H
 1456.


1457. H
 1458. H
 1459. CD₃
 243. 1460. H
 1461. H
 1462.


1463. H
 1464. H
 1465. CD₃
 244. 1466. H
 1467. H
 1468.


1469. H
 1470. H
 1471. CD₃
 245. 1472. H
 1473. H
 1474.


1475. H
 1476. H
 1477. CD₃
 246. 1478. H
 1479. H
 1480.


1481. H
 1482. H
 1483. CD₃
 247. 1484. H
 1485. H
 1486.


1487. H
 1488. H
 1489. CD₃
 248. 1490. H
 1491. H
 1492.


1493. H
 1494. H
 1495. CD₃
 249. 1496. H
 1497. H
 1498.


1499. H
 1500. H
 1501. CD₃
 250. 1502. H
 1503. H
 1504.


1505. H
 1506. H
 1507. CD₃
 251. 1508. H
 1509. H
 1510.


1511. H
 1512. H
 1513. CD₃
 252. 1514. H
 1515. H
 1516.


1517. H
 1518. H
 1519. CD₃
 253. 1520. H
 1521. H
 1522.


1523. H
 1524. H
 1525. CD₃
 254. 1526. H
 1527. H
 1528.


1529. H
 1530. H
 1531. CD₃
 255. 1532. H
 1533. H
 1534. CD₃
 1535. H
 1536. CD₃
 1537. CD₃
 256. 1538. H
 1539. H
 1540. CD₂CD₃
 1541. H
 1542. CD₃
 1543. CD₃
 257. 1544. H
 1545. H
 1546. CD₂CH₃
 1547. H
 1548. CD₃
 1549. CD₃
 258. 1550. H
 1551. H
 1552. CD(CD₃)₂
 1553. H
 1554. CD₃
 1555. CD₃
 259. 1556. H
 1557. H
 1558. CD(CH₃)₂
 1559. H
 1560. CD₃
 1561. CD₃
 260. 1562. H
 1563. H
 1564. CD₂CD(CD₃)₂
 1565. H
 1566. CD₃
 1567. CD₃
 261. 1568. H
 1569. H
 1570. CD₂CH(CH₃)₂
 1571. H
 1572. CD₃
 1573. CD₃
 262. 1574. H
 1575. H
 1576. CD₂C(CD₃)₃
 1577. H
 1578. CD₃
 1579. CD₃
 263. 1580. H
 1581. H
 1582. CD₂C(CH₃)₃
 1583. H
 1584. CD₃
 1585. CD₃
 264. 1586. H
 1587. H
 1588. CD₂CD₂CF₃
 1589. H
 1590. CD₃
 1591. CD₃
 265. 1592. H
 1593. H
 1594. CD₂CH₂CF₃
 1595. H
 1596. CD₃
 1597. CD₃
 266. 1598. H
 1599. H
 1600. CD₂CCF₃(CH₃)₂
 1601. H
 1602. CD₃
 1603. CD₃
 267. 1604. H
 1605. H
 1606.


1607. H
 1608. CD₃
 1609. CD₃
 268. 1610. H
 1611. H
 1612.


1613. H
 1614. CD₃
 1615. CD₃
 269. 1616. H
 1617. H
 1618.


1619. H
 1620. CD₃
 1621. CD₃
 270. 1622. H
 1623. H
 1624.


1625. H
 1626. CD₃
 1627. CD₃
 271. 1628. H
 1629. H
 1630.


1631. H
 1632. CD₃
 1633. CD₃
 272. 1634. H
 1635. H
 1636.


1637. H
 1638. CD₃
 1639. CD₃
 273. 1640. H
 1641. H
 1642.


1643. H
 1644. CD₃
 1645. CD₃
 274. 1646. H
 1647. H
 1648.


1649. H
 1650. CD₃
 1651. CD₃
 275. 1652. H
 1653. H
 1654.


1655. H
 1656. CD₃
 1657. CD₃
 276. 1658. H
 1659. H
 1660.


1661. H
 1662. CD₃
 1663. CD₃
 277. 1664. H
 1665. H
 1666.


1667. H
 1668. CD₃
 1669. CD₃
 278. 1670. H
 1671. H
 1672.


1673. H
 1674. CD₃
 1675. CD₃
 279. 1676. H
 1677. H
 1678.


1679. H
 1680. CD₃
 1681. CD₃
 280. 1682. H
 1683. H
 1684.


1685. H
 1686. CD₃
 1687. CD₃
 281. 1688. H
 1689. H
 1690.


1691. H
 1692. CD₃
 1693. CD₃
 282. 1694. H
 1695. H
 1696.


1697. H
 1698. CD₃
 1699. CD₃
 283. 1700. H
 1701. H
 1702.


1703. H
 1704. CD₃
 1705. CD₃
 284. 1706. H
 1707. H
 1708.


1709. H
 1710. CD₃
 1711. CD₃
 285. 1712. H
 1713. H
 1714.


1715. H
 1716. CD₃
 1717. CD₃
 286. 1718. H
 1719. H
 1720.


1721. H
 1722. CD₃
 1723. CD₃
 287. 1724. CD₃
 1725. H
 1726. CD₃
 1727. CD₃
 1728. CD₃
 1729. CD₃
 288. 1730. CD₃
 1731. H
 1732. CD₂CD₃
 1733. CD₃
 1734. CD₃
 1735. CD₃
 289. 1736. CD₃
 1737. H
 1738. CD₂CH₃
 1739. CD₃
 1740. CD₃
 1741. CD₃
 290. 1742. CD₃
 1743. H
 1744. CD(CD₃)₂
 1745. CD₃
 1746. CD₃
 1747. CD₃
 291. 1748. CD₃
 1749. H
 1750. CD(CH₃)₂
 1751. CD₃
 1752. CD₃
 1753. CD₃
 292. 1754. CD₃
 1755. H
 1756. CD₂CD(CD₃)₂
 1757. CD₃
 1758. CD₃
 1759. CD₃
 293. 1760. CD₃
 1761. H
 1762. CD₂CH(CH₃)₂
 1763. CD₃
 1764. CD₃
 1765. CD₃
 294. 1766. CD₃
 1767. H
 1768. CD₂C(CD₃)₃
 1769. CD₃
 1770. CD₃
 1771. CD₃
 295. 1772. CD₃
 1773. H
 1774. CD₂C(CH₃)₃
 1775. CD₃
 1776. CD₃
 1777. CD₃
 296. 1778. CD₃
 1779. H
 1780. CD₂CD₂CF₃
 1781. CD₃
 1782. CD₃
 1783. CD₃
 297. 1784. CD₃
 1785. H
 1786. CD₂CH₂CF₃
 1787. CD₃
 1788. CD₃
 1789. CD₃
 298. 1790. CD₃
 1791. H
 1792. CD₂CCF₃(CH₃)₂
 1793. CD₃
 1794. CD₃
 1795. CD₃
 299. 1796. CD₃
 1797. H
 1798.


1799. CD₃
 1800. CD₃
 1801. CD₃
 300. 1802. CD₃
 1803. H
 1804.


1805. CD₃
 1806. CD₃
 1807. CD₃
 301. 1808. CD₃
 1809. H
 1810.


1811. CD₃
 1812. CD₃
 1813. CD₃
 302. 1814. CD₃
 1815. H
 1816.


1817. CD₃
 1818. CD₃
 1819. CD₃
 303. 1820. CD₃
 1821. H
 1822.


1823. CD₃
 1824. CD₃
 1825. CD₃
 304. 1826. CD₃
 1827. H
 1828.


1829. CD₃
 1830. CD₃
 1831. CD₃
 305. 1832. CD₃
 1833. H
 1834.


1835. CD₃
 1836. CD₃
 1837. CD₃
 306. 1838. CD₃
 1839. H
 1840.


1841. CD₃
 1842. CD₃
 1843. CD₃
 307. 1844. CD₃
 1845. H
 1846.


1847. CD₃
 1848. CD₃
 1849. CD₃
 308. 1850. CD₃
 1851. H
 1852.


1853. CD₃
 1854. CD₃
 1855. CD₃
 309. 1856. CD₃
 1857. H
 1858.


1859. CD₃
 1860. CD₃
 1861. CD₃
 310. 1862. CD₃
 1863. H
 1864.


1865. CD₃
 1866. CD₃
 1867. CD₃
 311. 1868. CD₃
 1869. H
 1870.


1871. CD₃
 1872. CD₃
 1873. CD₃
 312. 1874. CD₃
 1875. H
 1876.


1877. CD₃
 1878. CD₃
 1879. CD₃
 313. 1880. CD₃
 1881. H
 1882.


1883. CD₃
 1884. CD₃
 1885. CD₃
 314. 1886. CD₃
 1887. H
 1888.


1889. CD₃
 1890. CD₃
 1891. CD₃
 315. 1892. CD₃
 1893. H
 1894.


1895. CD₃
 1896. CD₃
 1897. CD₃
 316. 1898. CD₃
 1899. H
 1900.


1901. CD₃
 1902. CD₃
 1903. CD₃
 317. 1904. CD₃
 1905. H
 1906.


1907. CD₃
 1908. CD₃
 1909. CD₃
 318. 1910. CD₃
 1911. H
 1912.


1913. CD₃
 1914. CD₃
 1915. CD₃
 319. 1916. CH₃
 1917. CH₂CH₃
 1918. CH₃
 1919. CH₃
 1920. H
 1921. CH₃
 320. 1922. CH₃
 1923. CH(CH₃)₂
 1924. CH₃
 1925. CH₃
 1926. 1927. CH₃
 321. 1928. CH₃
 1929. CH₂CH(CH₃)₂
 1930. CH₃
 1931. CH₃
 1932. H
 1933. CH₃
 322. 1934. CH₃
 1935. C(CH₃)₃
 1936. CH₃
 1937. CH₃
 1938. 1939. CH₃
 323. 1940. CH₃
 1941. CH₂C(CH₃)₃
 1942. CH₃
 1943. CH₃
 1944. H
 1945. CH₃
 324. 1946. CH₃
 1947. CH₂CH₂CF₃
 1948. CH₃
 1949. CH₃
 1950. 1951. CH₃
 325. 1952. CH₃
 1953. CH₂CCF₃(CH₃)₂
 1954. CH₃
 1955. CH₃
 1956. H
 1957. CH₃
 326. 1958. CH₃
 1959.


1960. CH₃
 1961. CH₃
 1962. 1963. CH₃
 327. 1964. CH₃
 1965.


1966. CH₃
 1967. CH₃
 1968. H
 1969. CH₃
 328. 1970. CH₃
 1971.


1972. CH₃
 1973. CH₃
 1974. 1975. CH₃
 329. 1976. CH₃
 1977.


1978. CH₃
 1979. CH₃
 1980. H
 1981. CH₃
 330. 1982. CH₃
 1983.


1984. CH₃
 1985. CH₃
 1986. 1987. CH₃
 331. 1988. CH₃
 1989.


1990. CH₃
 1991. CH₃
 1992. H
 1993. CH₃
 332. 1994. CH₃
 1995.


1996. CH₃
 1997. CH₃
 1998. 1999. CH₃
 333. 2000. CH₃
 2001.


2002. CH₃
 2003. CH₃
 2004. H
 2005. CH₃
 334. 2006. CH₃
 2007.


2008. CH₃
 2009. CH₃
 2010. 2011. CH₃
 335. 2012. CH₃
 2013.


2014. CH₃
 2015. CH₃
 2016. H
 2017. CH₃
 336. 2018. CH₃
 2019.


2020. CH₃
 2021. CH₃
 2022. 2023. CH₃
 337. 2024. CH₃
 2025.


2026. CH₃
 2027. CH₃
 2028. H
 2029. CH₃
 338. 2030. CH₃
 2031.


2032. CH₃
 2033. CH₃
 2034. 2035. CH₃
 339. 2036. CH₃
 2037.


2038. CH₃
 2039. CH₃
 2040. H
 2041. CH₃
 340. 2042. CH₃
 2043.


2044. CH₃
 2045. CH₃
 2046. 2047. CH₃
 341. 2048. CH₃
 2049.


2050. CH₃
 2051. CH₃
 2052. H
 2053. CH₃
 342. 2054. CH₃
 2055.


2056. CH₃
 2057. CH₃
 2058. 2059. CH₃
 343. 2060. CH₃
 2061.


2062. CH₃
 2063. CH₃
 2064. H
 2065. CH₃
 344. 2066. CH₃
 2067.


2068. CH₃
 2069. CH₃
 2070. 2071. CH₃
 345. 2072. CH₃
 2073.


2074. CH₃
 2075. CH₃
 2076. H
 2077. CH₃
 346. 2078. CD₃
 2079. CD₂CD₃
 2080. CD₃
 2081. CD₃
 2082. H
 2083. CD₃
 347. 2084. CD₃
 2085. CD₂CH₃
 2086. CD₃
 2087. CD₃
 2088. 2089. CD₃
 348. 2090. CD₃
 2091. CD(CD₃)₂
 2092. CD₃
 2093. CD₃
 2094. H
 2095. CD₃
 349. 2096. CD₃
 2097. CD(CH₃)₂
 2098. CD₃
 2099. CD₃
 2100. 2101. CD₃
 350. 2102. CD₃
 2103. CD₂CD(CD₃)₂
 2104. CD₃
 2105. CD₃
 2106. H
 2107. CD₃
 351. 2108. CD₃
 2109. CD₂CH(CH₃)₂
 2110. CD₃
 2111. CD₃
 2112. 2113. CD₃
 352. 2114. CD₃
 2115. CD₂C(CD₃)₃
 2116. CD₃
 2117. CD₃
 2118. H
 2119. CD₃
 353. 2120. CD₃
 2121. CD₂C(CH₃)₃
 2122. CD₃
 2123. CD₃
 2124. 2125. CD₃
 354. 2126. CD₃
 2127. CD₂CD₂CF₃
 2128. CD₃
 2129. CD₃
 2130. H
 2131. CD₃
 355. 2132. CD₃
 2133. CD₂CH₂CF₃
 2134. CD₃
 2135. CD₃
 2136. 2137. CD₃
 356. 2138. CD₃
 2139. CD₂CCF₃(CH₃)₂
 2140. CD₃
 2141. CD₃
 2142. H
 2143. CD₃
 357. 2144. CD₃
 2145.


2146. CD₃
 2147. CD₃
 2148. H
 2149. CD₃
 358. 2150. CD₃
 2151.


2152. CD₃
 2153. CD₃
 2154. H
 2155. CD₃
 359. 2156. CD₃
 2157.


2158. CD₃
 2159. CD₃
 2160. 2161. CD₃
 360. 2162. CD₃
 2163.


2164. CD₃
 2165. CD₃
 2166. H
 2167. CD₃
 361. 2168. CD₃
 2169.


2170. CD₃
 2171. CD₃
 2172. 2173. CD₃
 362. 2174. CD₃
 2175.


2176. CD₃
 2177. CD₃
 2178. H
 2179. CD₃
 363. 2180. CD₃
 2181.


2182. CD₃
 2183. CD₃
 2184. 2185. CD₃
 364. 2186. CD₃
 2187.


2188. CD₃
 2189. CD₃
 2190. H
 2191. CD₃
 365. 2192. CD₃
 2193.


2194. CD₃
 2195. CD₃
 2196. 2197. CD₃
 366. 2198. CD₃
 2199.


2200. CD₃
 2201. CD₃
 2202. H
 2203. CD₃
 367. 2204. CD₃
 2205.


2206. CD₃
 2207. CD₃
 2208. 2209. CD₃
 368. 2210. CD₃
 2211.


2212. CD₃
 2213. CD₃
 2214. H
 2215. CD₃
 369. 2216. CD₃
 2217.


2218. CD₃
 2219. CD₃
 2220. 2221. CD₃
 370. 2222. CD₃
 2223.


2224. CD₃
 2225. CD₃
 2226. H
 2227. CD₃
 371. 2228. CD₃
 2229.


2230. CD₃
 2231. CD₃
 2232. 2233. CD₃
 372. 2234. CD₃
 2235.


2236. CD₃
 2237. CD₃
 2238. H
 2239. CD₃
 373. 2240. CD₃
 2241.


2242. CD₃
 2243. CD₃
 2244. 2245. CD₃
 374. 2246. CD₃
 2247.


2248. CD₃
 2249. CD₃
 2250. H
 2251. CD₃
 375. 2252. CD₃
 2253.


2254. CD₃
 2255. CD₃
 2256. 2257. CD₃
 376. 2258. CD₃
 2259.


2260. CD₃
 2261. CD₃
 2262. H
 2263. CD₃
 377. 2264. CD₃
 2265. CD₂CD₃
 2266. CD₃
 2267. CD₃
 2268. CD₂CD₃
 2269. CD₃
 378. 2270. CD₃
 2271. CD₂CH₃
 2272. CD₃
 2273. CD₃
 2274. CD₂CD₃
 2275. CD₃
 379. 2276. CD₃
 2277. CD(CD₃)₂
 2278. CD₃
 2279. CD₃
 2280. CD₂CD₃
 2281. CD₃
 380. 2282. CD₃
 2283. CD(CH₃)₂
 2284. CD₃
 2285. CD₃
 2286. CD₂CD₃
 2287. CD₃
 381. 2288. CD₃
 2289. CD₂CD(CD₃)₂
 2290. CD₃
 2291. CD₃
 2292. CD₂CD₃
 2293. CD₃
 382. 2294. CD₃
 2295. CD₂CH(CH₃)₂
 2296. CD₃
 2297. CD₃
 2298. CD₂CD₃
 2299. CD₃
 383. 2300. CD₃
 2301. CD₂C(CD₃)₃
 2302. CD₃
 2303. CD₃
 2304. CD₂CD₃
 2305. CD₃
 384. 2306. CD₃
 2307. CD₂C(CH₃)₃
 2308. CD₃
 2309. CD₃
 2310. CD₂CD₃
 2311. CD₃
 385. 2312. CD₃
 2313. CD₂CD₂CF₃
 2314. CD₃
 2315. CD₃
 2316. CD₂CD₃
 2317. CD₃
 386. 2318. CD₃
 2319. CD₂CH₂CF₃
 2320. CD₃
 2321. CD₃
 2322. CD₂CD₃
 2323. CD₃
 387. 2324. CD₃
 2325. CD₂CCF₃(CH₃)₂
 2326. CD₃
 2327. CD₃
 2328. CD₂CD₃
 2329. CD₃
 388. 2330. CD₃
 2331.


2332. CD₃
 2333. CD₃
 2334. CD₂CD₃
 2335. CD₃
 389. 2336. CD₃
 2337.


2338. CD₃
 2339. CD₃
 2340. CD₂CD₃
 2341. CD₃
 390. 2342. CD₃
 2343.


2344. CD₃
 2345. CD₃
 2346. CD₂CD₃
 2347. CD₃
 391. 2348. CD₃
 2349.


2350. CD₃
 2351. CD₃
 2352. CD₂CD₃
 2353. CD₃
 392. 2354. CD₃
 2355.


2356. CD₃
 2357. CD₃
 2358. CD₂CD₃
 2359. CD₃
 393. 2360. CD₃
 2361.


2362. CD₃
 2363. CD₃
 2364. CD₂CD₃
 2365. CD₃
 394. 2366. CD₃
 2367.


2368. CD₃
 2369. CD₃
 2370. CD₂CD₃
 2371. CD₃
 395. 2372. CD₃
 2373.


2374. CD₃
 2375. CD₃
 2376. CD₂CD₃
 2377. CD₃
 396. 2378. CD₃
 2379.


2380. CD₃
 2381. CD₃
 2382. CD₂CD₃
 2383. CD₃
 397. 2384. CD₃
 2385.


2386. CD₃
 2387. CD₃
 2388. CD₂CD₃
 2389. CD₃
 398. 2390. CD₃
 2391.


2392. CD₃
 2393. CD₃
 2394. CD₂CD₃
 2395. CD₃
 399. 2396. CD₃
 2397.


2398. CD₃
 2399. CD₃
 2400. CD₂CD₃
 2401. CD₃
 400. 2402. CD₃
 2403.


2404. CD₃
 2405. CD₃
 2406. CD₂CD₃
 2407. CD₃
 401. 2408. CD₃
 2409.


2410. CD₃
 2411. CD₃
 2412. CD₂CD₃
 2413. CD₃
 402. 2414. CD₃
 2415.


2416. CD₃
 2417. CD₃
 2418. CD₂CD₃
 2419. CD₃
 403. 2420. CD₃
 2421.


2422. CD₃
 2423. CD₃
 2424. CD₂CD₃
 2425. CD₃
 404. 2426. CD₃
 2427.


2428. CD₃
 2429. CD₃
 2430. CD₂CD₃
 2431. CD₃
 405. 2432. CD₃
 2433.


2434. CD₃
 2435. CD₃
 2436. CD₂CD₃
 2437. CD₃
 406. 2438. CD₃
 2439.


2440. CD₃
 2441. CD₃
 2442. CD₂CD₃
 2443. CD₃
 407. 2444. CD₃
 2445.


2446. CD₃
 2447. CD₃
 2448. CD₂CD₃
 2449. CD₃
 408. 2450. CH₃
 2451. CH₃
 2452. H
 2453. H
 2454. H
 2455. CH₃
 409. 2456. CH₃
 2457. CH₂CH₃
 2458. H
 2459. H
 2460. H
 2461. CH₃
 410. 2462. CH₃
 2463. CH(CH₃)₂
 2464. H
 2465. H
 2466. H
 2467. CH₃
 411. 2468. CH₃
 2469. CH₂CH(CH₃)₂
 2470. H
 2471. H
 2472. H
 2473. CH₃
 412. 2474. CH₃
 2475. C(CH₃)₃
 2476. H
 2477. H
 2478. H
 2479. CH₃
 413. 2480. CH₃
 2481. CH₂C(CH₃)₃
 2482. H
 2483. H
 2484. H
 2485. CH₃
 414. 2486. CH₃
 2487. CH₂CH₂CF₃
 2488. H
 2489. H
 2490. H
 2491. CH₃
 415. 2492. CH₃
 2493. CH₂CCF₃(CH₃)₂
 2494. H
 2495. H
 2496. H
 2497. CH₃
 416. 2498. CH₃
 2499.


2500. H
 2501. H
 2502. H
 2503. CH₃
 417. 2504. CH₃
 2505.


2506. H
 2507. H
 2508. H
 2509. CH₃
 418. 2510. CH₃
 2511.


2512. H
 2513. H
 2514. H
 2515. CH₃
 419. 2516. CH₃
 2517.


2518. H
 2519. H
 2520. H
 2521. CH₃
 420. 2522. CH₃
 2523.


2524. H
 2525. H
 2526. H
 2527. CH₃
 421. 2528. CH₃
 2529.


2530. H
 2531. H
 2532. H
 2533. CH₃
 422. 2534. CH₃
 2535.


2536. H
 2537. H
 2538. H
 2539. CH₃
 423. 2540. CH₃
 2541.


2542. H
 2543. H
 2544. H
 2545. CH₃
 424. 2546. CH₃
 2547.


2548. H
 2549. H
 2550. H
 2551. CH₃
 425. 2552. CH₃
 2553.


2554. H
 2555. H
 2556. H
 2557. CH₃
 426. 2558. CH₃
 2559.


2560. H
 2561. H
 2562. H
 2563. CH₃
 427. 2564. CH₃
 2565.


2566. H
 2567. H
 2568. H
 2569. CH₃
 428. 2570. CH₃
 2571.


2572. H
 2573. H
 2574. H
 2575. CH₃
 429. 2576. CH₃
 2577.


2578. H
 2579. H
 2580. H
 2581. CH₃
 430. 2582. CH₃
 2583.


2584. H
 2585. H
 2586. H
 2587. CH₃
 431. 2588. CH₃
 2589.


2590. H
 2591. H
 2592. H
 2593. CH₃
 432. 2594. CH₃
 2595.


2596. H
 2597. H
 2598. H
 2599. CH₃
 433. 2600. CH₃
 2601.


2602. H
 2603. H
 2604. H
 2605. CH₃
 434. 2606. CH₃
 2607.


2608. H
 2609. H
 2610. H
 2611. CH₃
 435. 2612. CH₃
 2613.


2614. H
 2615. H
 2616. H
 2617. CH₃
 436. 2618. CD₃
 2619. CD₃
 2620. H
 2621. H
 2622. H
 2623. CD₂CD₃
 437. 2624. CD₃
 2625. CD₂CD₃
 2626. H
 2627. H
 2628. H
 2629. CD₂CD₃
 438. 2630. CD₃
 2631. CD₂CH₃
 2632. H
 2633. H
 2634. H
 2635. CD₂CD₃
 439. 2636. CD₃
 2637. CD(CD₃)₂
 2638. H
 2639. H
 2640. H
 2641. CD₂CD₃
 440. 2642. CD₃
 2643. CD(CH₃)₂
 2644. H
 2645. H
 2646. H
 2647. CD₂CD₃
 441. 2648. CD₃
 2649. CD₂CD(CD₃)₂
 2650. H
 2651. H
 2652. H
 2653. CD₂CD₃
 442. 2654. CD₃
 2655. CD₂CH(CH₃)₂
 2656. H
 2657. H
 2658. H
 2659. CD₂CD₃
 443. 2660. CD₃
 2661. CD₂C(CD₃)₃
 2662. H
 2663. H
 2664. H
 2665. CD₂CD₃
 444. 2666. CD₃
 2667. CD₂C(CH₃)₃
 2668. H
 2669. H
 2670. H
 2671. CD₂CD₃
 445. 2672. CD₃
 2673. CD₂CD₂CF₃
 2674. H
 2675. H
 2676. H
 2677. CD₂CD₃
 446. 2678. CD₃
 2679. CD₂CH₂CF₃
 2680. H
 2681. H
 2682. H
 2683. CD₂CD₃
 447. 2684. CD₃
 2685. CD₂CCF₃(CH₃)₂
 2686. H
 2687. H
 2688. H
 2689. CD₂CD₃
 448. 2690. CD₃
 2691.


2692. H
 2693. H
 2694. H
 2695. CD₂CD₃
 449. 2696. CD₃
 2697.


2698. H
 2699. H
 2700. H
 2701. CD₂CD₃
 450. 2702. CD₃
 2703.


2704. H
 2705. H
 2706. H
 2707. CD₂CD₃
 451. 2708. CD₃
 2709.


2710. H
 2711. H
 2712. H
 2713. CD₂CD₃
 452. 2714. CD₃
 2715.


2716. H
 2717. H
 2718. H
 2719. CD₂CD₃
 453. 2720. CD₃
 2721.


2722. H
 2723. H
 2724. H
 2725. CD₂CD₃
 454. 2726. CD₃
 2727.


2728. H
 2729. H
 2730. H
 2731. CD₂CD₃
 455. 2732. CD₃
 2733.


2734. H
 2735. H
 2736. H
 2737. CD₂CD₃
 456. 2738. CD₃
 2739.


2740. H
 2741. H
 2742. H
 2743. CD₂CD₃
 457. 2744. CD₃
 2745.


2746. H
 2747. H
 2748. H
 2749. CD₂CD₃
 458. 2750. CD₃
 2751.


2752. H
 2753. H
 2754. H
 2755. CD₂CD₃
 459. 2756. CD₃
 2757.


2758. H
 2759. H
 2760. H
 2761. CD₂CD₃
 460. 2762. CD₃
 2763.


2764. H
 2765. H
 2766. H
 2767. CD₂CD₃
 461. 2768. CD₃
 2769.


2770. H
 2771. H
 2772. H
 2773. CD₂CD₃
 462. 2774. CD₃
 2775.


2776. H
 2777. H
 2778. H
 2779. CD₂CD₃
 463. 2780. CD₃
 2781.


2782. H
 2783. H
 2784. H
 2785. CD₂CD₃
 464. 2786. CD₃
 2787.


2788. H
 2789. H
 2790. H
 2791. CD₂CD₃
 465. 2792. CD₃
 2793.


2794. H
 2795. H
 2796. H
 2797. CD₂CD₃
 466. 2798. CD₃
 2799.


2800. H
 2801. H
 2802. H
 2803. CD₂CD₃
 467. 2804. CD₃
 2805.


2806. H
 2807. H
 2808. H
 2809. CD₂CD₃
 468. 2810. CH₃
 2811. H
 2812. CH₃
 2813. H
 2814. H
 2815. CH₃
 469. 2816. CH₃
 2817. H
 2818. CH₂CH₃
 2819. H
 2820. H
 2821. CH₃
 470. 2822. CH₃
 2823. H
 2824. CH(CH₃)₂
 2825. H
 2826. H
 2827. CH₃
 471. 2828. CH₃
 2829. H
 2830. CH₂CH(CH₃)₂
 2831. H
 2832. H
 2833. CH₃
 472. 2834. CH₃
 2835. H
 2836. C(CH₃)₃
 2837. H
 2838. H
 2839. CH₃
 473. 2840. CH₃
 2841. H
 2842. CH₂C(CH₃)₃
 2843. H
 2844. H
 2845. CH₃
 474. 2846. CH₃
 2847. H
 2848. CH₂CH₂CF₃
 2849. H
 2850. H
 2851. CH₃
 475. 2852. CH₃
 2853. H
 2854. CH₂CCF₃(CH₃)₂
 2855. H
 2856. H
 2857. CH₃
 476. 2858. CH₃
 2859. H
 2860.


2861. H
 2862. H
 2863. CH₃
 477. 2864. CH₃
 2865. H
 2866.


2867. H
 2868. H
 2869. CH₃
 478. 2870. CH₃
 2871. H
 2872.


2873. H
 2874. H
 2875. CH₃
 479. 2876. CH₃
 2877. H
 2878.


2879. H
 2880. H
 2881. CH₃
 480. 2882. CH₃
 2883. H
 2884.


2885. H
 2886. H
 2887. CH₃
 481. 2888. CH₃
 2889. H
 2890.


2891. H
 2892. H
 2893. CH₃
 482. 2894. CH₃
 2895. H
 2896.


2897. H
 2898. H
 2899. CH₃
 483. 2900. CH₃
 2901. H
 2902.


2903. H
 2904. H
 2905. CH₃
 484. 2906. CH₃
 2907. H
 2908.


2909. H
 2910. H
 2911. CH₃
 485. 2912. CH₃
 2913. H
 2914.


2915. H
 2916. H
 2917. CH₃
 486. 2918. CH₃
 2919. H
 2920.


2921. H
 2922. H
 2923. CH₃
 487. 2924. CH₃
 2925. H
 2926.


2927. H
 2928. H
 2929. CH₃
 488. 2930. CH₃
 2931. H
 2932.


2933. H
 2934. H
 2935. CH₃
 489. 2936. CH₃
 2937. H
 2938.


2939. H
 2940. H
 2941. CH₃
 490. 2942. CH₃
 2943. H
 2944.


2945. H
 2946. H
 2947. CH₃
 491. 2948. CH₃
 2949. H
 2950.


2951. H
 2952. H
 2953. CH₃
 492. 2954. CH₃
 2955. H
 2956.


2957. H
 2958. H
 2959. CH₃
 493. 2960. CH₃
 2961. H
 2962.


2963. H
 2964. H
 2965. CH₃
 494. 2966. CH₃
 2967. H
 2968.


2969. H
 2970. H
 2971. CH₃
 495. 2972. CH₃
 2973. H
 2974.


2975. H
 2976. H
 2977. CH₃
 496. 2978. CD₃
 2979. H
 2980. CD₃
 2981. H
 2982. H
 2983. CD₂CD₃
 497. 2984. CD₃
 2985. H
 2986. CD₂CD₃
 2987. H
 2988. H
 2989. CD₂CD₃
 498. 2990. CD₃
 2991. H
 2992. CD₂CH₃
 2993. H
 2994. H
 2995. CD₂CD₃
 499. 2996. CD₃
 2997. H
 2998. CD(CD₃)₂
 2999. H
 3000. H
 3001. CD₂CD₃
 500. 3002. CD₃
 3003. H
 3004. CD(CH₃)₂
 3005. H
 3006. H
 3007. CD₂CD₃
 501. 3008. CD₃
 3009. H
 3010. CD₂CD(CD₃)₂
 3011. H
 3012. H
 3013. CD₂CD₃
 502. 3014. CD₃
 3015. H
 3016. CD₂CH(CH₃)₂
 3017. H
 3018. H
 3019. CD₂CD₃
 503. 3020. CD₃
 3021. H
 3022. CD₂C(CD₃)₃
 3023. H
 3024. H
 3025. CD₂CD₃
 504. 3026. CD₃
 3027. H
 3028. CD₂C(CH₃)₃
 3029. H
 3030. H
 3031. CD₂CD₃
 505. 3032. CD₃
 3033. H
 3034. CD₂CD₂CF₃
 3035. H
 3036. H
 3037. CD₂CD₃
 506. 3038. CD₃
 3039. H
 3040. CD₂CH₂CF₃
 3041. H
 3042. H
 3043. CD₂CD₃
 507. 3044. CD₃
 3045. H
 3046. CD₂CCF₃(CH₃)₂
 3047. H
 3048. H
 3049. CD₂CD₃
 508. 3050. CD₃
 3051. H
 3052.


3053. H
 3054. H
 3055. CD₂CD₃
 509. 3056. CD₃
 3057. H
 3058.


3059. H
 3060. H
 3061. CD₂CD₃
 510. 3062. CD₃
 3063. H
 3064.


3065. H
 3066. H
 3067. CD₂CD₃
 511. 3068. CD₃
 3069. H
 3070.

3071 H
 3072. H
 3073. CD₂CD₃
 512. 3074. CD₃
 3075. H
 3076.


3077. H
 3078. H
 3079. CD₂CD₃
 513. 3080. CD₃
 3081. H
 3082.


3083. H
 3084. H
 3085. CD₂CD₃
 514. 3086. CD₃
 3087. H
 3088.


3089. H
 3090. H
 3091. CD₂CD₃
 515. 3092. CD₃
 3093. H
 3094.


3095. H
 3096. H
 3097. CD₂CD₃
 516. 3098. CD₃
 3099. H
 3100.


3101. H
 3102. H
 3103. CD₂CD₃
 517. 3104. CD₃
 3105. H
 3106.


3107. H
 3108. H
 3109. CD₂CD₃
 518. 3110. CD₃
 3111. H
 3112.


3113. H
 3114. H
 3115. CD₂CD₃
 519. 3116. CD₃
 3117. H
 3118.


3119. H
 3120. H
 3121. CD₂CD₃
 520. 3122. CD₃
 3123. H
 3124.


3125. H
 3126. H
 3127. CD₂CD₃
 521. 3128. CD₃
 3129. H
 3130.


3131. H
 3132. H
 3133. CD₂CD₃
 522. 3134. CD₃
 3135. H
 3136.


3137. H
 3138. H
 3139. CD₂CD₃
 523. 3140. CD₃
 3141. H
 3142.


3143. H
 3144. H
 3145. CD₂CD₃
 524. 3146. CD₃
 3147. H
 3148.


3149. H
 3150. H
 3151. CD₂CD₃
 525. 3152. CD₃
 3153. H
 3154.


3155. H
 3156. H
 3157. CD₂CD₃
 526. 3158. CD₃
 3159. H
 3160.


3161. H
 3162. H
 3163. CD₂CD₃
 527. 3164. CD₃
 3165. H
 3166.


3167. H
 3168. H
 3169. CD₂CD₃
 528. 3170. CH(CH₃)₂
 3171. H
 3172. H
 3173. CH₃
 3174. CH₃
 3175. CH₃
 529. 3176. CH(CH₃)₂
 3177. H
 3178. H
 3179. CH₂CH₃
 3180. CH₃
 3181. CH₃
 530. 3182. CH(CH₃)₂
 3183. H
 3184. H
 3185. CH(CH₃)₂
 3186. CH₃
 3187. CH₃
 531. 3188. CH(CH₃)₂
 3189. H
 3190. H
 3191. CH₂CH(CH₃)₂
 3192. CH₃
 3193. CH₃
 532. 3194. CH(CH₃)₂
 3195. H
 3196. H
 3197. C(CH₃)₃
 3198. CH₃
 3199. CH₃
 533. 3200. CH(CH₃)₂
 3201. H
 3202. H
 3203. CH₂C(CH₃)₃
 3204. CH₃
 3205. CH₃
 534. 3206. CH(CH₃)₂
 3207. H
 3208. H
 3209. CH₂CH₂CF₃
 3210. CH₃
 3211. CH₃
 535. 3212. CH(CH₃)₂
 3213. H
 3214. H
 3215. CH₂CCF₃(CH₃)₂
 3216. CH₃
 3217. CH₃
 536. 3218. CH(CH₃)₂
 3219. H
 3220. H
 3221.


3222. CH₃
 3223. CH₃
 537. 3224. CH(CH₃)₂
 3225. H
 3226. H
 3227.


3228. CH₃
 3229. CH₃
 538. 3230. CH(CH₃)₂
 3231. H
 3232. H
 3233.


3234. CH₃
 3235. CH₃
 539. 3236. CH(CH₃)₂
 3237. H
 3238. H
 3239.


3240. CH₃
 3241. CH₃
 540. 3242. CH(CH₃)₂
 3243. H
 3244. H
 3245.


3246. CH₃
 3247. CH₃
 541. 3248. CH(CH₃)₂
 3249. H
 3250. H
 3251.


3252. CH₃
 3253. CH₃
 542. 3254. CH(CH₃)₂
 3255. H
 3256. H
 3257.


3258. CH₃
 3259. CH₃
 543. 3260. CH(CH₃)₂
 3261. H
 3262. H
 3263.


3264. CH₃
 3265. CH₃
 544. 3266. CH(CH₃)₂
 3267. H
 3268. H
 3269.


3270. CH₃
 3271. CH₃
 545. 3272. CH(CH₃)₂
 3273. H
 3274. H
 3275.


3276. CH₃
 3277. CH₃
 546. 3278. CH(CH₃)₂
 3279. H
 3280. H
 3281.


3282. CH₃
 3283. CH₃
 547. 3284. CH(CH₃)₂
 3285. H
 3286. H
 3287.


3288. CH₃
 3289. CH₃
 548. 3290. CH(CH₃)₂
 3291. H
 3292. H
 3293.


3294. CH₃
 3295. CH₃
 549. 3296. CH(CH₃)₂
 3297. H
 3298. H
 3299.


3300. CH₃
 3301. CH₃
 550. 3302. CH(CH₃)₂
 3303. H
 3304. H
 3305.


3306. CH₃
 3307. CH₃
 551. 3308. CH(CH₃)₂
 3309. H
 3310. H
 3311.


3312. CH₃
 3313. CH₃
 552. 3314. CH(CH₃)₂
 3315. H
 3316. H
 3317.


3318. CH₃
 3319. CH₃
 553. 3320. CH(CH₃)₂
 3321. H
 3322. H
 3323.


3324. CH₃
 3325. CH₃
 554. 3326. CH(CH₃)₂
 3327. H
 3328. H
 3329.


3330. CH₃
 3331. CH₃
 555. 3332. CH(CH₃)₂
 3333. H
 3334. H
 3335.


3336. CH₃
 3337. CH₃
 556. 3338. CD₃
 3339. H
 3340. H
 3341. CD₃
 3342. CD₃
 3343. CD₃
 557. 3344. CD₃
 3345. H
 3346. H
 3347. CD₂CD₃
 3348. CD₃
 3349. CD₃
 558. 3350. CD₃
 3351. H
 3352. H
 3353. CD₂CH₃
 3354. CD₃
 3355. CD₃
 559. 3356. CD₃
 3357. H
 3358. H
 3359. CD(CD₃)₂
 3360. CD₃
 3361. CD₃
 560. 3362. CD₃
 3363. H
 3364. H
 3365. CD(CH₃)₂
 3366. CD₃
 3367. CD₃
 561. 3368. CD₃
 3369. H
 3370. H
 3371. CD₂CD(CD₃)₂
 3372. CD₃
 3373. CD₃
 562. 3374. CD₃
 3375. H
 3376. H
 3377. CD₂CH(CH₃)₂
 3378. CD₃
 3379. CD₃
 563. 3380. CD₃
 3381. H
 3382. H
 3383. CD₂C(CD₃)₃
 3384. CD₃
 3385. CD₃
 564. 3386. CD₃
 3387. H
 3388. H
 3389. CD₂C(CH₃)₃
 3390. CD₃
 3391. CD₃
 565. 3392. CD₃
 3393. H
 3394. H
 3395. CD₂CD₂CF₃
 3396. CD₃
 3397. CD₃
 566. 3398. CD₃
 3399. H
 3400. H
 3401. CD₂CH₂CF₃
 3402. CD₃
 3403. CD₃
 567. 3404. CD₃
 3405. H
 3406. H
 3407. CD₂CCF₃(CH₃)₂
 3408. CD₃
 3409. CD₃
 568. 3410. CD₃
 3411. H
 3412. H
 3413.


3414. CD₃
 3415. CD₃
 569. 3416. CD₃
 3417. H
 3418. H
 3419.


3420. CD₃
 3421. CD₃
 570. 3422. CD₃
 3423. H
 3424. H
 3425.


3426. CD₃
 3427. CD₃
 571. 3428. CD₃
 3429. H
 3430. H
 3431.


3432. CD₃
 3433. CD₃
 572. 3434. CD₃
 3435. H
 3436. H
 3437.


3438. CD₃
 3439. CD₃
 573. 3440. CD₃
 3441. H
 3442. H
 3443.


3444. CD₃
 3445. CD₃
 574. 3446. CD₃
 3447. H
 3448. H
 3449.


3450. CD₃
 3451. CD₃
 575. 3452. CD₃
 3453. H
 3454. H
 3455.


3456. CD₃
 3457. CD₃
 576. 3458. CD₃
 3459. H
 3460. H
 3461.


3462. CD₃
 3463. CD₃
 577. 3464. CD₃
 3465. H
 3466. H
 3467.


3468. CD₃
 3469. CD₃
 578. 3470. CD₃
 3471. H
 3472. H
 3473.


3474. CD₃
 3475. CD₃
 579. 3476. CD₃
 3477. H
 3478. H
 3479.


3480. CD₃
 3481. CD₃
 580. 3482. CD₃
 3483. H
 3484. H
 3485.


3486. CD₃
 3487. CD₃
 581. 3488. CD₃
 3489. H
 3490. H
 3491.


3492. CD₃
 3493. CD₃
 582. 3494. CD₃
 3495. H
 3496. H
 3497.


3498. CD₃
 3499. CD₃
 583. 3500. CD₃
 3501. H
 3502. H
 3503.


3504. CD₃
 3505. CD₃
 584. 3506. CD₃
 3507. H
 3508. H
 3509.


3510. CD₃
 3511. CD₃
 585. 3512. CD₃
 3513. H
 3514. H
 3515.


3516. CD₃
 3517. CD₃
 586. 3518. CD₃
 3519. H
 3520. H
 3521.


3522. CD₃
 3523. CD₃
 587. 3524. CD₃
 3525. H
 3526. H
 3527.


3528. CD₃
 3529. CD₃
 588. 3530. H
 3531. CH₃
 3532. CH₃
 3533. H
 3534. CH₃
 3535. CH₃
 589. 3536. H
 3537. CH₂CH₃
 3538. CH₃
 3539. H
 3540. CH₃
 3541. CH₃
 590. 3542. H
 3543. CH(CH₃)₂
 3544. CH₃
 3545. H
 3546. CH₃
 3547. CH₃
 591. 3548. H
 3549. CH₂CH(CH₃)₂
 3550. CH₃
 3551. H
 3552. CH₃
 3553. CH₃
 592. 3554. H
 3555. C(CH₃)₃
 3556. CH₃
 3557. H
 3558. CH₃
 3559. CH₃
 593. 3560. H
 3561. CH₂C(CH₃)₃
 3562. CH₃
 3563. H
 3564. CH₃
 3565. CH₃
 594. 3566. H
 3567. CH₂CH₂CF₃
 3568. CH₃
 3569. H
 3570. CH₃
 3571. CH₃
 595. 3572. H
 3573. CH₂CCF₃(CH₃)₂
 3574. CH₃
 3575. H
 3576. CH₃
 3577. CH₃
 596. 3578. H
 3579.


3580. CH₃
 3581. H
 3582. CH₃
 3583. CH₃
 597. 3584. H
 3585.


3586. CH₃
 3587. H
 3588. CH₃
 3589. CH₃
 598. 3590. H
 3591.


3592. CH₃
 3593. H
 3594. CH₃
 3595. CH₃
 599. 3596. H
 3597.


3598. CH₃
 3599. H
 3600. CH₃
 3601. CH₃
 600. 3602. H
 3603.


3604. CH₃
 3605. H
 3606. CH₃
 3607. CH₃
 601. 3608. H
 3609.


3610. CH₃
 3611. H
 3612. CH₃
 3613. CH₃
 602. 3614. H
 3615.


3616. CH₃
 3617. H
 3618. CH₃
 3619. CH₃
 603. 3620. H
 3621.


3622. CH₃
 3623. H
 3624. CH₃
 3625. CH₃
 604. 3626. H
 3627.


3628. CH₃
 3629. H
 3630. CH₃
 3631. CH₃
 605. 3632. H
 3633.


3634. CH₃
 3635. H
 3636. CH₃
 3637. CH₃
 606. 3638. H
 3639.


3640. CH₃
 3641. H
 3642. CH₃
 3643. CH₃
 607. 3644. H
 3645.


3646. CH₃
 3647. H
 3648. CH₃
 3649. CH₃
 608. 3650. H
 3651.


3652. CH₃
 3653. H
 3654. CH₃
 3655. CH₃
 609. 3656. H
 3657.


3658. CH₃
 3659. H
 3660. CH₃
 3661. CH₃
 610. 3662. H
 3663.


3664. CH₃
 3665. H
 3666. CH₃
 3667. CH₃
 611. 3668. H
 3669.


3670. CH₃
 3671. H
 3672. CH₃
 3673. CH₃
 612. 3674. H
 3675.


3676. CH₃
 3677. H
 3678. CH₃
 3679. CH₃
 613. 3680. H
 3681.


3682. CH₃
 3683. H
 3684. CH₃
 3685. CH₃
 614. 3686. H
 3687.


3688. CH₃
 3689. H
 3690. CH₃
 3691. CH₃
 615. 3692. H
 3693.


3694. CH₃
 3695. H
 3696. CH₃
 3697. CH₃
 616. 3698. CD3
 3699. CD₃
 3700. CD₃
 3701. H
 3702. CD₃
 3703. CD₃
 617. 3704. CD3
 3705. CD₂CD₃
 3706. CD₃
 3707. H
 3708. CD₃
 3709. CD₃
 618. 3710. CD3
 3711. CD₂CH₃
 3712. CD₃
 3713. H
 3714. CD₃
 3715. CD₃
 619. 3716. CD3
 3717. CD(CD₃)₂
 3718. CD₃
 3719. H
 3720. CD₃
 3721. CD₃
 620. 3722. CD3
 3723. CD(CH₃)₂
 3724. CD₃
 3725. H
 3726. CD₃
 3727. CD₃
 621. 3728. CD3
 3729. CD₂CD(CD₃)₂
 3730. CD₃
 3731. H
 3732. CD₃
 3733. CD₃
 622. 3734. CD3
 3735. CD₂CH(CH₃)₂
 3736. CD₃
 3737. H
 3738. CD₃
 3739. CD₃
 623. 3740. CD3
 3741. CD₂C(CD₃)₃
 3742. CD₃
 3743. H
 3744. CD₃
 3745. CD₃
 624. 3746. CD₃
 3747. CD₂C(CH₃)₃
 3748. CD₃
 3749. H
 3750. CD₃
 3751. CD₃
 625. 3752. CD₃
 3753. CD₂CD₂CF₃
 3754. CD₃
 3755. H
 3756. CD₃
 3757. CD₃
 626. 3758. CD₃
 3759. CD₂CH₂CF₃
 3760. CD₃
 3761. H
 3762. CD₃
 3763. CD₃
 627. 3764. CD₃
 3765. CD₂CCF₃(CH₃)₂
 3766. CD₃
 3767. H
 3768. CD₃
 3769. CD₃
 628. 3770. CD₃
 3771.


3772. CD₃
 3773. H
 3774. CD₃
 3775. CD₃
 629. 3776. CD₃
 3777.


3778. CD₃
 3779. H
 3780. CD₃
 3781. CD₃
 630. 3782. CD₃
 3783.


3784. CD₃
 3785. H
 3786. CD₃
 3787. CD₃
 631. 3788. CD₃
 3789.


3790. CD₃
 3791. H
 3792. CD₃
 3793. CD₃
 632. 3794. CD₃
 3795.


3796. CD₃
 3797. H
 3798. CD₃
 3799. CD₃
 633. 3800. CD₃
 3801.


3802. CD₃
 3803. H
 3804. CD₃
 3805. CD₃
 634. 3806. CD₃
 3807.


3808. CD₃
 3809. H
 3810. CD₃
 3811. CD₃
 635. 3812. CD₃
 3813.


3814. CD₃
 3815. H
 3816. CD₃
 3817. CD₃
 636. 3818. CD₃
 3819.


3820. CD₃
 3821. H
 3822. CD₃
 3823. CD₃
 637. 3824. CD₃
 3825.


3826. CD₃
 3827. H
 3828. CD₃
 3829. CD₃
 638. 3830. CD₃
 3831.


3832. CD₃
 3833. H
 3834. CD₃
 3835. CD₃
 639. 3836. CD₃
 3837.


3838. CD₃
 3839. H
 3840. CD₃
 3841. CD₃
 640. 3842. CD₃
 3843.


3844. CD₃
 3845. H
 3846. CD₃
 3847. CD₃
 641. 3848. CD₃
 3849.


3850. CD₃
 3851. H
 3852. CD₃
 3853. CD₃
 642. 3854. CD₃
 3855.


3856. CD₃
 3857. H
 3858. CD₃
 3859. CD₃
 643. 3860. CD₃
 3861.


3862. CD₃
 3863. H
 3864. CD₃
 3865. CD₃
 644. 3866. CD₃
 3867.


3868. CD₃
 3869. H
 3870. CD₃
 3871. CD₃
 645. 3872. CD₃
 3873.


3874. CD₃
 3875. H
 3876. CD₃
 3877. CD3
 646. 3878. CD₃
 3879.


3880. CD₃
 3881. H
 3882. CD₃
 3883. CD₃
 647. 3884. CD₃
 3885.


3886. CD₃
 3887. H
 3888. CD₃
 3889. CD₃
 648. 3890. CH₃
 3891. CH₃
 3892. CH₂CH₃
 3893. H
 3894. CH₃
 3895. CH₂CH₃
 649. 3896. CH₃
 3897. CH₃
 3898. CH(CH₃)₂
 3899. H
 3900. CH₃
 3901. CH₂CH₃
 650. 3902. CH₃
 3903. CH₃
 3904. CH₂CH(CH₃)₂
 3905. H
 3906. CH₃
 3907. CH₂CH₃
 651. 3908. CH₃
 3909. CH₃
 3910. C(CH₃)₃
 3911. H
 3912. CH₃
 3913. CH₂CH₃
 652. 3914. CH₃
 3915. CH₃
 3916. CH₂C(CH₃)₃
 3917. H
 3918. CH₃
 3919. CH₂CH₃
 653. 3920. CH₃
 3921. CH₃
 3922. CH₂CH₂CF₃
 3923. H
 3924. CH₃
 3925. CH₂CH₃
 654. 3926. CH₃
 3927. CH₃
 3928. CH₂CCF₃(CH₃)₂
 3929. H
 3930. CH₃
 3931. CH₂CH₃
 655. 3932. CH₃
 3933. CH₃
 3934.


3935. H
 3936. CH₃
 3937. CH₂CH₃
 656. 3938. CH₃
 3939. CH₃
 3940.


3941. H
 3942. CH₃
 3943. CH₂CH₃
 657. 3944. CH₃
 3945. CH₃
 3946.


3947. H
 3948. CH₃
 3949. CH₂CH₃
 658. 3950. CH₃
 3951. CH₃
 3952.


3953. H
 3954. CH₃
 3955. CH₂CH₃
 659. 3956. CH₃
 3957. CH₃
 3958.


3959. H
 3960. CH₃
 3961. CH₂CH₃
 660. 3962. CH₃
 3963. CH₃
 3964.


3965. H
 3966. CH₃
 3967. CH₂CH₃
 661. 3968. CH₃
 3969. CH₃
 3970.


3971. H
 3972. CH₃
 3973. CH₂CH₃
 662. 3974. CH₃
 3975. CH₃
 3976.


3977. H
 3978. CH₃
 3979. CH₂CH₃
 663. 3980. CH₃
 3981. CH₃
 3982.


3983. H
 3984. CH₃
 3985. CH₂CH₃
 664. 3986. CH₃
 3987. CH₃
 3988.


3989. H
 3990. CH₃
 3991. CH₂CH₃
 665. 3992. CH₃
 3993. CH₃
 3994.


3995. H
 3996. CH₃
 3997. CH₂CH₃
 666. 3998. CH₃
 3999. CH₃
 4000.


4001. H
 4002. CH₃
 4003. CH₂CH₃
 667. 4004. CH₃
 4005. CH₃
 4006.


4007. H
 4008. CH₃
 4009. CH₂CH₃
 668. 4010. CH₃
 4011. CH₃
 4012.


4013. H
 4014. CH₃
 4015. CH₂CH₃
 669. 4016. CH₃
 4017. CH₃
 4018.


4019. H
 4020. CH₃
 4021. CH₂CH₃
 670. 4022. CH₃
 4023. CH₃
 4024.


4025. H
 4026. CH₃
 4027. CH₂CH₃
 671. 4028. CH₃
 4029. CH₃
 4030.


4031. H
 4032. CH₃
 4033. CH₂CH₃
 672. 4034. CH₃
 4035. CH₃
 4036.


4037. H
 4038. CH₃
 4039. CH₂CH₃
 673. 4040. CH₃
 4041. CH₃
 4042.


4043. H
 4044. CH₃
 4045. CH₂CH₃
 674. 4046. CH₃
 4047. CH₃
 4048.


4049. H
 4050. CH₃
 4051. CH₂CH₃
 675. 4052. CD₃
 4053. CD₃
 4054. CD₂CD₃
 4055. H
 4056. CD₂CH₃
 4057. CD₂CH₃
 676. 4058. CD₃
 4059. CD₃
 4060. CD₂CH₃
 4061. H
 4062. CD₂CH₃
 4063. CD₂CH₃
 677. 4064. CD₃
 4065. CD₃
 4066. CD(CD₃)₂
 4067. H
 4068. CD₂CH₃
 4069. CD₂CH₃
 678. 4070. CD₃
 4071. CD₃
 4072. CD(CH₃)₂
 4073. H
 4074. CD₂CH₃
 4075. CD₂CH₃
 679. 4076. CD₃
 4077. CD₃
 4078. CD₂CD(CD₃)₂
 4079. H
 4080. CD₂CH₃
 4081. CD₂CH₃
 680. 4082. CD₃
 4083. CD₃
 4084. CD₂CH(CH₃)₂
 4085. H
 4086. CD₂CH₃
 4087. CD₂CH₃
 681. 4088. CD₃
 4089. CD₃
 4090. CD₂C(CD₃)₃
 4091. H
 4092. CD₂CH₃
 4093. CD₂CH₃
 682. 4094. CD₃
 4095. CD₃
 4096. CD₂C(CH₃)₃
 4097. H
 4098. CD₂CH₃
 4099. CD₂CH₃
 683. 4100. CD₃
 4101. CD₃
 4102. CD₂CD₂CF₃
 4103. H
 4104. CD₂CH₃
 4105. CD₂CH₃
 684. 4106. CD₃
 4107. CD₃
 4108. CD₂CH₂CF₃
 4109. H
 4110. CD₂CH₃
 4111. CD₂CH₃
 685. 4112. CD₃
 4113. CD₃
 4114. CD₂CCF₃(CH₃)₂
 4115. H
 4116. CD₂CH₃
 4117. CD₂CH₃
 686. 4118. CD₃
 4119. CD₃
 4120.


4121. H
 4122. CD₂CH₃
 4123. CD₂CH₃
 687. 4124. CD₃
 4125. CD₃
 4126.


4127. H
 4128. CD₂CH₃
 4129. CD₂CH₃
 688. 4130. CD₃
 4131. CD₃
 4132.


4133. H
 4134. CD₂CH₃
 4135. CD₂CH₃
 689. 4136. CD₃
 4137. CD₃ 4138 .


4139. H
 4140. CD₂CH₃
 4141. CD₂CH₃
 690. 4142. CD₃
 4143. CD₃
 4144.


4145. H
 4146. CD₂CH₃
 4147. CD₂CH₃
 691. 4148. CD₃
 4149. CD₃
 4150.


4151. H
 4152. CD₂CH₃
 4153. CD₂CH₃
 692. 4154. CD₃
 4155. CD₃
 4156.


4157. H
 4158. CD₂CH₃
 4159. CD₂CH₃
 693. 4160. CD₃
 4161. CD₃
 4162.


4163. H
 4164. CD₂CH₃
 4165. CD₂CH₃
 694. 4166. CD₃
 4167. CD₃
 4168.


4169. H
 4170. CD₂CH₃
 4171. CD₂CH₃
 695. 4172. CD₃
 4173. CD₃
 4174.


4175. H
 4176. CD₂CH₃
 4177. CD₂CH₃
 696. 4178. CD₃
 4179. CD₃
 4180.


4181. H
 4182. CD₂CH₃
 4183. CD₂CH₃
 697. 4184. CD₃
 4185. CD₃
 4186.


4187. H
 4188. CD₂CH₃
 4189. CD₂CH₃
 698. 4190. CD₃
 4191. CD₃
 4192.


4193. H
 4194. CD₂CH₃
 4195. CD₂CH₃
 699. 4196. CD₃
 4197. CD₃
 4198.


4199. H
 4200. CD₂CH₃
 4201. CD₂CH₃
 700. 4202. CD₃
 4203. CD₃
 4204.


4205. H
 4206. CD₂CH₃
 4207. CD₂CH₃
 701. 4208. CD₃
 4209. CD₃
 4210.


4211. H
 4212. CD₂CH₃
 4213. CD₂CH₃
 702. 4214. CD₃
 4215. CD₃
 4216.


4217. H
 4218. CD₂CH₃
 4219. CD₂CH₃
 703. 4220. CD₃
 4221. CD₃
 4222.


4223. H
 4224. CD₂CH₃
 4225. CD₂CH₃
 704. 4226. CD₃
 4227. CD₃
 4228.


4229. H
 4230. CD₂CH₃
 4231. CD₂CH₃
 705. 4232. CD₃
 4233. CD₃
 4234.


4235. H
 4236. CD₂CH₃
 4237. CD₂CH₃
 706. 4238. H
 4239. CH₃
 4240. CH₃
 4241. CH₃
 4242. CH₂CH₃
 4243. CH₂CH₃
 707. 4244. H
 4245. CH₃
 4246. CH₂CH₃
 4247. CH₃
 4248. CH₂CH₃
 4249. CH₂CH₃
 708. 4250. H
 4251. CH₃
 4252. CH(CH₃)₂
 4253. CH₃
 4254. CH₂CH₃
 4255. CH₂CH₃
 709. 4256. H
 4257. CH₃
 4258. CH₂CH(CH₃)₂
 4259. CH₃
 4260. CH₂CH₃
 4261. CH₂CH₃
 710. 4262. H
 4263. CH₃
 4264. C(CH₃)₃
 4265. CH₃
 4266. CH₂CH₃
 4267. CH₂CH₃
 711. 4268. H
 4269. CH₃
 4270. CH₂C(CH₃)₃
 4271. CH₃
 4272. CH₂CH₃
 4273. CH₂CH₃
 712. 4274. H
 4275. CH₃
 4276. CH₂CH₂CF₃
 4277. CH₃
 4278. CH₂CH₃
 4279. CH₂CH₃
 713. 4280. H
 4281. CH₃
 4282. CH₂CCF₃(CH₃)₂
 4283. CH₃
 4284. CH₂CH₃
 4285. CH₂CH₃
 714. 4286. H
 4287. CH₃
 4288.


4289. CH₃
 4290. CH₂CH₃
 4291. CH₂CH₃
 715. 4292. H
 4293. CH₃
 4294.


4295. CH₃
 4296. CH₂CH₃
 4297. CH₂CH₃
 716. 4298. H
 4299. CH₃
 4300.


4301. CH₃
 4302. CH₂CH₃
 4303. CH₂CH₃
 717. 4304. H
 4305. CH₃ 4306


4307. CH₃
 4308. CH₂CH₃
 4309. CH₂CH₃
 718. 4310. H
 4311. CH₃
 4312.


4313. CH₃
 4314. CH₂CH₃
 4315. CH₂CH₃
 719. 4316. H
 4317. CH₃
 4318.


4319. CH₃
 4320. CH₂CH₃
 4321. CH₂CH₃
 720. 4322. H
 4323. CH₃
 4324.


4325. CH₃
 4326. CH₂CH₃
 4327. CH₂CH₃
 721. 4328. H
 4329. CH₃
 4330.


4331. CH₃
 4332. CH₂CH₃
 4333. CH₂CH₃
 722. 4334. H
 4335. CH₃
 4336.


4337. CH₃
 4338. CH₂CH₃
 4339. CH₂CH₃
 723. 4340. H
 4341. CH₃
 4342.


4343. CH₃
 4344. CH₂CH₃
 4345. CH₂CH₃
 724. 4346. H
 4347. CH₃
 4348.


4349. CH₃
 4350. CH₂CH₃
 4351. CH₂CH₃
 725. 4352. H
 4353. CH₃
 4354.


4355. CH₃
 4356. CH₂CH₃
 4357. CH₂CH₃
 726. 4358. H
 4359. CH₃
 4360.


4361. CH₃
 4362. CH₂CH₃
 4363. CH₂CH₃
 727. 4364. H
 4365. CH₃
 4366.


4367. CH₃
 4368. CH₂CH₃
 4369. CH₂CH₃
 728. 4370. H
 4371. CH₃
 4372.


4373. CH₃
 4374. CH₂CH₃
 4375. CH₂CH₃
 729. 4376. H
 4377. CH₃
 4378.


4379. CH₃
 4380. CH₂CH₃
 4381. CH₂CH₃
 730. 4382. H
 4383. CH₃
 4384.


4385. CH₃
 4386. CH₂CH₃
 4387. CH₂CH₃
 731. 4388. H
 4389. CH₃
 4390.


4391. CH₃
 4392. CH₂CH₃
 4393. CH₂CH₃
 732. 4394. H
 4395. CH₃
 4396.


4397. CH₃
 4398. CH₂CH₃
 4399. CH₂CH₃
 733. 4400. H
 4401. CH₃
 4402.


4403. CH₃
 4404. CH₂CH₃
 4405. CH₂CH₃
 734. 4406. CD₃
 4407. CD₃
 4408. CD₃
 4409. CD₃
 4410. CD₂CH₃
 4411. CD₂CH₃
 735. 4412. CD₃
 4413. CD₃
 4414. CD₂CD₃
 4415. CD₃
 4416. CD₂CH₃
 4417. CD₂CH₃
 736. 4418. CD₃
 4419. CD₃
 4420. CD₂CH₃
 4421. CD₃
 4422. CD₂CH₃
 4423. CD₂CH₃
 737. 4424. CD₃
 4425. CD₃
 4426. CD(CD₃)₂
 4427. CD₃
 4428. CD₂CH₃
 4429. CD₂CH₃
 738. 4430. CD₃
 4431. CD₃
 4432. CD(CH₃)₂
 4433. CD₃
 4434. CD₂CH₃
 4435. CD₂CH₃
 739. 4436. CD₃
 4437. CD₃
 4438. CD₂CD(CD₃)₂
 4439. CD₃
 4440. CD₂CH₃
 4441. CD₂CH₃
 740. 4442. CD₃
 4443. CD₃
 4444. CD₂CH(CH₃)₂
 4445. CD₃
 4446. CD₂CH₃
 4447. CD₂CH₃
 741. 4448. CD₃
 4449. CD₃
 4450. CD₂C(CD₃)₃
 4451. CD₃
 4452. CD₂CH₃
 4453. CD₂CH₃
 742. 4454. CD₃
 4455. CD₃
 4456. CD₂C(CH₃)₃
 4457. CD₃
 4458. CD₂CH₃
 4459. CD₂CH₃
 743. 4460. CD₃
 4461. CD₃
 4462. CD₂CD₂CF₃
 4463. CD₃
 4464. CD₂CH₃
 4465. CD₂CH₃
 744. 4466. CD₃
 4467. CD₃
 4468. CD₂CH₂CF₃
 4469. CD₃
 4470. CD₂CH₃
 4471. CD₂CH₃
 745. 4472. CD₃
 4473. CD₃
 4474. CD₂CCF₃(CH₃)₂
 4475. CD₃
 4476. CD₂CH₃
 4477. CD₂CH₃
 746. 4478. CD₃
 4479. CD₃
 4480.


4481. CD₃
 4482. CD₂CH₃
 4483. CD₂CH₃
 747. 4484. CD₃
 4485. CD₃
 4486.


4487. CD₃
 4488. CD₂CH₃
 4489. CD₂CH₃
 748. 4490. CD₃
 4491. CD₃ 4492


4493. CD₃
 4494. CD₂CH₃
 4495. CD₂CH₃
 749. 4496. CD₃
 4497. CD₃ 4498 .


4499. CD₃
 4500. CD₂CH₃
 4501. CD₂CH₃
 750. 4502. CD₃
 4503. CD₃
 4504.


4505. CD₃
 4506. CD₂CH₃
 4507. CD₂CH₃
 751. 4508. CD₃
 4509. CD₃ 4510


4511. CD₃
 4512. CD₂CH₃
 4513. CD₂CH₃
 752. 4514. CD₃
 4515. CD₃
 4516.


4517. CD₃
 4518. CD₂CH₃
 4519. CD₂CH₃
 753. 4520. CD₃
 4521. CD₃
 4522.


4523. CD₃
 4524. CD₂CH₃
 4525. CD₂CH₃
 754. 4526. CD₃
 4527. CD₃
 4528.


4529. CD₃
 4530. CD₂CH₃
 4531. CD₂CH₃
 755. 4532. CD₃
 4533. CD₃
 4534.


4535. CD₃
 4536. CD₂CH₃
 4537. CD₂CH₃
 756. 4538. CD₃
 4539. CD₃
 4540.


4541. CD₃
 4542. CD₂CH₃
 4543. CD₂CH₃
 757. 4544. CD₃
 4545. CD₃
 4546.


4547. CD₃
 4548. CD₂CH₃
 4549. CD₂CH₃
 758. 4550. CD₃
 4551. CD₃
 4552.


4553. CD₃
 4554. CD₂CH₃
 4555. CD₂CH₃
 759. 4556. CD₃
 4557. CD₃
 4558.


4559. CD₃
 4560. CD₂CH₃
 4561. CD₂CH₃
 760. 4562. CD₃
 4563. CD₃
 4564.


4565. CD₃
 4566. CD₂CH₃
 4567. CD₂CH₃
 761. 4568. CD₃
 4569. CD₃
 4570.


4571. CD₃
 4572. CD₂CH₃
 4573. CD₂CH₃
 762. 4574. CD₃
 4575. CD₃
 4576.


4577. CD₃
 4578. CD₂CH₃
 4579. CD₂CH₃
 763. 4580. CD₃
 4581. CD₃
 4582.


4583. CD₃
 4584. CD₂CH₃
 4585. CD₂CH₃
 764. 4586. CD₃
 4587. CD₃
 4588.


4589. CD₃
 4590. CD₂CH₃
 4591. CD₂CH₃
 765. 4592. CD₃
 4593. CD₃
 4594.


4595. CD₃
 4596. CD₂CH₃
 4597. CD₂CH₃
 766. 4598. CH₃
 4599. CH₂CH₃
 4600. CH₃
 4601. CH₂CH₃
 4602. H
 4603. CH₂CH₃
 767. 4604. CH₃
 4605. CH(CH₃)₂
 4606. CH₃
 4607. CH(CH₃)₂
 4608. H
 4609. CH₂CH₃
 768. 4610. CH₃
 4611. CH₂CH(CH₃)₂
 4612. CH₃
 4613. CH₂CH(CH₃)₂
 4614. H
 4615. CH₂CH₃
 769. 4616. CH₃
 4617. C(CH₃)₃
 4618. CH₃
 4619. C(CH₃)₃
 4620. H
 4621. CH₂CH₃
 770. 4622. CH₃
 4623. CH₂C(CH₃)₃
 4624. CH₃
 4625. CH₂C(CH₃)₃
 4626. H
 4627. CH₂CH₃
 771. 4628. CH₃
 4629. CH₂CH₂CF₃
 4630. CH₃
 4631. CH₂CH₂CF₃
 4632. H
 4633. CH₂CH₃
 772. 4634. CH₃
 4635. CH₂CCF₃(CH₃)₂
 4636. CH₃
 4637. CH₂CCF₃(CH₃)₂
 4638. H
 4639. CH₂CH₃
 773. 4640. CH₃
 4641.


4642. CH₃
 4643.


4644. H
 4645. CH₂CH₃
 774. 4646. CH₃
 4647.


4648. CH₃
 4649.


4650. H
 4651. CH₂CH₃
 775. 4652. CH₃
 4653.


4654. CH₃
 4655.


4656. H
 4657. CH₂CH₃
 776. 4658. CH₃
 4659.


4660. CH₃
 4661.


4662. H
 4663. CH₂CH₃
 777. 4664. CH₃
 4665.


4666. CH₃
 4667.


4668. H
 4669. CH₂CH₃
 778. 4670. CH₃
 4671.


4672. CH₃
 4673.


4674. H
 4675. CH₂CH₃
 779. 4676. CH₃
 4677.


4678. CH₃
 4679.


4680. H
 4681. CH₂CH₃
 780. 4682. CH₃
 4683.


4684. CH₃
 4685.


4686. H
 4687. CH₂CH₃
 781. 4688. CH₃
 4689.


4690. CH₃
 4691.


4692. H
 4693. CH₂CH₃
 782. 4694. CH₃
 4695.


4696. CH₃
 4697.


4698. H
 4699. CH₂CH₃
 783. 4700. CH₃
 4701.


4702. CH₃
 4703.


4704. H
 4705. CH₂CH₃
 784. 4706. CH₃
 4707.


4708. CH₃
 4709.


4710. H
 4711. CH₂CH₃
 785. 4712. CH₃
 4713.


4714. CH₃
 4715.


4716. H
 4717. CH₂CH₃
 786. 4718. CH₃
 4719.


4720. CH₃
 4721.


4722. H
 4723. CH₂CH₃
 787. 4724. CH₃
 4725.


4726. CH₃
 4727.


4728. H
 4729. CH₂CH₃
 788. 4730. CH₃
 4731.


4732. CH₃
 4733.


4734. H
 4735. CH₂CH₃
 789. 4736. CH₃
 4737.


4738. CH₃
 4739.


4740. H
 4741. CH₂CH₃
 790. 4742. CH₃
 4743.


4744. CH₃
 4745.


4746. H
 4747. CH₂CH₃
 791. 4748. CH₃
 4749.


4750. CH₃
 4751.


4752. H
 4753. CH₂CH₃
 792. 4754. CH₃
 4755.


4756. CH₃
 4757.


4758. H
 4759. CH₂CH₃
 793. 4760. CD₃
 4761. CD₂CD₃
 4762. CD₃
 4763. CD₂CD₃
 4764. H
 4765. CD₂CH₃
 794. 4766. CD₃
 4767. CD₂CH₃
 4768. CD₃
 4769. CD₂CH₃
 4770. H
 4771. CD₂CH₃
 795. 4772. CD₃
 4773. CD(CD₃)₂
 4774. CD₃
 4775. CD(CD₃)₂
 4776. H
 4777. CD₂CH₃
 796. 4778. CD₃
 4779. CD(CH₃)₂
 4780. CD₃
 4781. CD(CH₃)₂
 4782. H
 4783. CD₂CH₃
 797. 4784. CD₃
 4785. CD₂CD(CD₃)₂
 4786. CD₃
 4787. CD₂CD(CD₃)₂
 4788. H
 4789. CD₂CH₃
 798. 4790. CD₃
 4791. CD₂CH(CH₃)₂
 4792. CD₃
 4793. CD₂CH(CH₃)₂
 4794. H
 4795. CD₂CH₃
 799. 4796. CD₃
 4797. CD₂C(CD₃)₃
 4798. CD₃
 4799. CD₂C(CD₃)₃
 4800. H
 4801. CD₂CH₃
 800. 4802. CD₃
 4803. CD₂C(CH₃)₃
 4804. CD₃
 4805. CD₂C(CH₃)₃
 4806. H
 4807. CD₂CH₃
 801. 4808. CD₃
 4809. CD₂CD₂CF₃
 4810. CD₃
 4811. CD₂CD₂CF₃
 4812. H
 4813. CD₂CH₃
 802. 4814. CD₃
 4815. CD₂CH₂CF₃
 4816. CD₃
 4817. CD₂CH₂CF₃
 4818. H
 4819. CD₂CH₃
 803. 4820. CD₃
 4821. CD₂CCF₃(CH₃)₂
 4822. CD₃
 4823. CD₂CCF₃(CH₃)₂
 4824. H
 4825. CD₂CH₃
 804. 4826. CD₃
 4827.


4828. CD₃
 4829.


4830. H
 4831. CD₂CH₃
 805. 4832. CD₃
 4833.


4834. CD₃
 4835.


4836. H
 4837. CD₂CH₃
 806. 4838. CD₃
 4839.


4840. CD₃
 4841.


4842. H
 4843. CD₂CH₃
 807. 4844. CD₃
 4845.


4846. CD₃
 4847.


4848. H
 4849. CD₂CH₃
 808. 4850. CD₃
 4851.


4852. CD₃
 4853.


4854. H
 4855. CD₂CH₃
 809. 4856. CD₃
 4857.


4858. CD₃
 4859.


4860. H
 4861. CD₂CH₃
 810. 4862. CD₃
 4863.


4864. CD₃
 4865.


4866. H
 4867. CD₂CH₃
 811. 4868. CD₃
 4869.


4870. CD₃
 4871.


4872. H
 4873. CD₂CH₃
 812. 4874. CD₃
 4875.


4876. CD₃
 4877.


4878. H
 4879. CD₂CH₃
 813. 4880. CD₃
 4881.


4882. CD₃
 4883.


4884. H
 4885. CD₂CH₃
 814. 4886. CD₃
 4887.


4888. CD₃
 4889.


4890. H
 4891. CD₂CH₃
 815. 4892. CD₃
 4893.


4894. CD₃
 4895.


4896. H
 4897. CD₂CH₃
 816. 4898. CD₃
 4899.


4900. CD₃
 4901.


4902. H
 4903. CD₂CH₃
 817. 4904. CD₃
 4905.


4906. CD₃
 4907.


4908. H
 4909. CD₂CH₃
 818. 4910. CD₃
 4911.


4912. CD₃
 4913.


4914. H
 4915. CD₂CH₃
 819. 4916. CD₃
 4917.


4918. CD₃
 4919.


4920. H
 4921. CD₂CH₃
 820. 4922. CD₃
 4923.


4924. CD₃
 4925.


4926. H
 4927. CD₂CH₃
 821. 4928. CD₃
 4929.


4930. CD₃
 4931.


4932. H
 4933. CD₂CH₃
 822. 4934. CD₃
 4935.


4936. CD₃
 4937.


4938. H
 4939. CD₂CH₃
 823. 4940. CD₃
 4941.


4942. CD₃
 4943.


4944. H
 4945. CD₂CH₃
 824. 4946. CH₂CH₃
 4947. CH₃
 4948. H
 4949. H
 4950. H
 4951. CH(CH₃)₂
 825. 4952. CH₂CH₃
 4953. CH₂CH₃
 4954. H
 4955. H
 4956. H
 4957. CH(CH₃)₂
 826. 4958. CH₂CH₃
 4959. CH(CH₃)₂
 4960. H
 4961. H
 4962. H
 4963. CH(CH₃)₂
 827. 4964. CH₂CH₃
 4965. CH₂CH(CH₃)₂
 4966. H
 4967. H
 4968. H
 4969. CH(CH₃)₂
 828. 4970. CH₂CH₃
 4971. C(CH₃)₃
 4972. H
 4973. H
 4974. H
 4975. CH(CH₃)₂
 829. 4976. CH₂CH₃
 4977. CH₂C(CH₃)₃
 4978. H
 4979. H
 4980. H
 4981. CH(CH₃)₂
 830. 4982. CH₂CH₃
 4983. CH₂CH₂CF₃
 4984. H
 4985. H
 4986. H
 4987. CH(CH₃)₂
 831. 4988. CH₂CH₃
 4989. CH₂CCF₃(CH₃)₂
 4990. H
 4991. H
 4992. H
 4993. CH(CH₃)₂
 832. 4994. CH₂CH₃
 4995.


4996. H
 4997. H
 4998. H
 4999. CH(CH₃)₂
 833. 5000. CH₂CH₃
 5001.


5002. H
 5003. H
 5004. H
 5005. CH(CH₃)₂
 834. 5006. CH₂CH₃
 5007.


5008. H
 5009. H
 5010. H
 5011. CH(CH₃)₂
 835. 5012. CH₂CH₃
 5013.


5014. H
 5015. H
 5016. H
 5017. CH(CH₃)₂
 836. 5018. CH₂CH₃
 5019.


5020. H
 5021. H
 5022. H
 5023. CH(CH₃)₂
 837. 5024. CH₂CH₃
 5025.


5026. H
 5027. H
 5028. H
 5029. CH(CH₃)₂
 838. 5030. CH₂CH₃
 5031.


5032. H
 5033. H
 5034. H
 5035. CH(CH₃)₂
 839. 5036. CH₂CH₃
 5037.


5038. H
 5039. H
 5040. H
 5041. CH(CH₃)₂
 840. 5042. CH₂CH₃
 5043.


5044. H
 5045. H
 5046. H
 5047. CH(CH₃)₂
 841. 5048. CH₂CH₃
 5049.


5050. H
 5051. H
 5052. H
 5053. CH(CH₃)₂
 842. 5054. CH₂CH₃
 5055.


5056. H
 5057. H
 5058. H
 5059. CH(CH₃)₂
 843. 5060. CH₂CH₃
 5061.


5062. H
 5063. H
 5064. H
 5065. CH(CH₃)₂
 844. 5066. CH₂CH₃
 5067.


5068. H
 5069. H
 5070. H
 5071. CH(CH₃)₂
 845. 5072. CH₂CH₃
 5073.


5074. H
 5075. H
 5076. H
 5077. CH(CH₃)₂
 846. 5078. CH₂CH₃
 5079.


5080. H
 5081. H
 5082. H
 5083. CH(CH₃)₂
 847. 5084. CH₂CH₃
 5085.


5086. H
 5087. H
 5088. H
 5089. CH(CH₃)₂
 848. 5090. CH₂CH₃
 5091.


5092. H
 5093. H
 5094. H
 5095. CH(CH₃)₂
 849. 5096. CH₂CH₃
 5097.


5098. H
 5099. H
 5100. H
 5101. CH(CH₃)₂
 850. 5102. CH₂CH₃
 5103.


5104. H
 5105. H
 5106. H
 5107. CH(CH₃)₂
 851. 5108. CH₂CH₃
 5109.


5110. H
 5111. H
 5112. H
 5113. CH(CH₃)₂
 852. 5114. CD₂CH₃
 5115. CD₃
 5116. H
 5117. H
 5118. CD₂CH₃
 5119. CD₂CH₃
 853. 5120. CD₂CH₃
 5121. CD₂CD₃
 5122. H
 5123. H
 5124. CD₂CH₃
 5125. CD₂CH₃
 854. 5126. CD₂CH₃
 5127. CD₂CH₃
 5128. H
 5129. H
 5130. CD₂CH₃
 5131. CD₂CH₃
 855. 5132. CD₂CH₃
 5133. CD(CD₃)₂
 5134. H
 5135. H
 5136. CD₂CH₃
 5137. CD₂CH₃
 856. 5138. CD₂CH₃
 5139. CD(CH₃)₂
 5140. H
 5141. H
 5142. CD₂CH₃
 5143. CD₂CH₃
 857. 5144. CD₂CH₃
 5145. CD₂CD(CD₃)₂
 5146. H
 5147. H
 5148. CD₂CH₃
 5149. CD₂CH₃
 858. 5150. CD₂CH₃
 5151. CD₂CH(CH₃)₂
 5152. H
 5153. H
 5154. CD₂CH₃
 5155. CD₂CH₃
 859. 5156. CD₂CH₃
 5157. CD₂C(CD₃)₃
 5158. H
 5159. H
 5160. CD₂CH₃
 5161. CD₂CH₃
 860. 5162. CD₂CH₃
 5163. CD₂C(CH₃)₃
 5164. H
 5165. H
 5166. CD₂CH₃
 5167. CD₂CH₃
 861. 5168. CD₂CH₃
 5169. CD₂CD₂CF₃
 5170. H
 5171. H
 5172. CD₂CH₃
 5173. CD₂CH₃
 862. 5174. CD₂CH₃
 5175. CD₂CH₂CF₃
 5176. H
 5177. H
 5178. CD₂CH₃
 5179. CD₂CH₃
 863. 5180. CD₂CH₃
 5181. CD₂CCF₃(CH₃)₂
 5182. H
 5183. H
 5184. CD₂CH₃
 5185. CD₂CH₃
 864. 5186. CD₂CH₃
 5187.


5188. H
 5189. H
 5190. CD₂CH₃
 5191. CD₂CH₃
 865. 5192. CD₂CH₃
 5193.


5194. H
 5195. H
 5196. CD₂CH₃
 5197. CD₂CH₃
 866. 5198. CD₂CH₃
 5199.


5200. H
 5201. H
 5202. CD₂CH₃
 5203. CD₂CH₃
 867. 5204. CD₂CH₃
 5205.


5206. H
 5207. H
 5208. CD₂CH₃
 5209. CD₂CH₃
 868. 5210. CD₂CH₃
 5211.


5212. H
 5213. H
 5214. CD₂CH₃
 5215. CD₂CH₃
 869. 5216. CD₂CH₃
 5217.


5218. H
 5219. H
 5220. CD₂CH₃
 5221. CD₂CH₃
 870. 5222. CD₂CH₃
 5223.


5224. H
 5225. H
 5226. CD₂CH₃
 5227. CD₂CH₃
 871. 5228. CD₂CH₃
 5229.


5230. H
 5231. H
 5232. CD₂CH₃
 5233. CD₂CH₃
 872. 5234. CD₂CH₃
 5235.


5236. H
 5237. H
 5238. CD₂CH₃
 5239. CD₂CH₃
 873. 5240. CD₂CH₃
 5241.


5242. H
 5243. H
 5244. CD₂CH₃
 5245. CD₂CH₃
 874. 5246. CD₂CH₃
 5247.


5248. H
 5249. H
 5250. CD₂CH₃
 5251. CD₂CH₃
 875. 5252. CD₂CH₃
 5253.


5254. H
 5255. H
 5256. CD₂CH₃
 5257. CD₂CH₃
 876. 5258. CD₂CH₃
 5259.


5260. H
 5261. H
 5262. CD₂CH₃
 5263. CD₂CH₃
 877. 5264. CD₂CH₃
 5265.


5266. H
 5267. H
 5268. CD₂CH₃
 5269. CD₂CH₃
 878. 5270. CD₂CH₃
 5271.


5272. H
 5273. H
 5274. CD₂CH₃
 5275. CD₂CH₃
 879. 5276. CD₂CH₃
 5277.


5278. H
 5279. H
 5280. CD₂CH₃
 5281. CD₂CH₃
 880. 5282. CD₂CH₃
 5283.


5284. H
 5285. H
 5286. CD₂CH₃
 5287. CD₂CH₃
 881. 5288. CD₂CH₃
 5289.


5290. H
 5291. H
 5292. CD₂CH₃
 5293. CD₂CH₃
 882. 5294. CD₂CH₃
 5295.


5296. H
 5297. H
 5298. CD₂CH₃
 5299. CD₂CH₃
 883. 5300. CD₂CH₃
 5301.


5302. H
 5303. H
 5304. CD₂CH₃
 5305. CD₂CH₃
 884. 5306. CD₂CH₃
 5307. CD₃
 5308. H
 5309. H
 5310. H
 5311. CD(CH₃)₂
 885. 5312. CD₂CH₃
 5313. CD₂CD₃
 5314. H
 5315. H
 5316. H
 5317. CD(CH₃)₂
 886. 5318. CD₂CD₃
 5319. CD₂CH₃
 5320. H
 5321. H
 5322. H
 5323. CD(CH₃)₂
 887. 5324. CD₂CD₃
 5325. CD(CD₃)₂
 5326. H
 5327. H
 5328. H
 5329. CD(CH₃)₂
 888. 5330. CD₂CD₃
 5331. CD(CD₃)₂
 5332. H
 5333. H
 5334. H
 5335. CD(CH₃)₂
 889. 5336. CD₂CD₃
 5337. CD₂CD(CD₃)₂
 5338. H
 5339. H
 5340. H
 5341. CD(CH₃)₂
 890. 5342. CD₂CD₃
 5343. CD₂CD(CH₃)₂
 5344. H
 5345. H
 5346. H
 5347. CD(CH₃)₂
 891. 5348. CD₂CD₃
 5349. CD₂C(CD₃)₃
 5350. H
 5351. H
 5352. H
 5353. CD(CH₃)₂
 892. 5354. CD₂CD₃
 5355. CD₂C(CH₃)₃
 5356. H
 5357. H
 5358. H
 5359. CD(CH₃)₂
 893. 5360. CD₂CD₃
 5361. CD₂CD₂CF₃
 5362. H
 5363. H
 5364. H
 5365. CD(CH₃)₂
 894. 5366. CD₂CD₃
 5367. CD₂CD₂CF₃
 5368. H
 5369. H
 5370. H
 5371. CD(CH₃)₂
 895. 5372. CD₂CD₃
 5373. CD₂CCF₃(CH₃)₂
 5374. H
 5375. H
 5376. H
 5377. CD(CH₃)₂
 896. 5378. CD₂CD₃
 5379.


5380. H
 5381. H
 5382. H
 5383. CD(CH₃)₂
 897. 5384. CD₂CD₃
 5385.


5386. H
 5387. H
 5388. H
 5389. CD(CH₃)₂
 898. 5390. CD₂CD₃
 5391.


5392. H
 5393. H
 5394. H
 5395. CD(CH₃)₂
 899. 5396. CD₂CD₃
 5397.


5398. H
 5399. H
 5400. H
 5401. CD(CH₃)₂
 900. 5402. CD₂CD₃
 5403.


5404. H
 5405. H
 5406. H
 5407. CD(CH₃)₂
 901. 5408. CD₂CD₃
 5409.


5410. H
 5411. H
 5412. H
 5413. CD(CH₃)₂
 902. 5414. CD₂CD₃
 5415.


5416. H
 5417. H
 5418. H
 5419. CD(CH₃)₂
 903. 5420. CD₂CD₃
 5421.


5422. H
 5423. H
 5424. H
 5425. CD(CH₃)₂
 904. 5426. CD₂CD₃
 5427.


5428. H
 5429. H
 5430. H
 5431. CD(C H₃)₂
 905. 5432. CD₂CD₃
 5433.


5434. H
 5435. H
 5436. H
 5437. CD(CH₃)₂
 906. 5438. CD₂CD₃
 5439.


5440. H
 5441. H
 5442. H
 5443. CD(CH₃)₂
 907. 5444. CD₂CD₃
 5445.


5446. H
 5447. H
 5448. H
 5449. CD(CH₃)₂
 908. 5450. CD₂CD₃
 5451.


5452. H
 5453. H
 5454. H
 5455. CD(CH₃)₂
 909. 5456. CD₂CD₃
 5457.


5458. H
 5459. H
 5460. H
 5461. CD(CH₃)₂
 910. 5462. CD₂CD₃
 5463.


5464. H
 5465. H
 5466. H
 5467. CD(CH₃)₂
 911. 5468. CD₂CD₃
 5469.


5470. H
 5471. H
 5472. H
 5473. CD(CH₃)₂
 912. 5474. CD₂CD₃
 5475.


5476. H
 5477. H
 5478. H
 5479. CD(CH₃)₂
 913. 5480. CD₂CD₃
 5481.


5482. H
 5483. H
 5484. H
 5485. CD(CH₃)₂
 914. 5486. CD₂CD₃
 5487.


5488. H
 5489. H
 5490. H
 5491. CD(CH₃)₂
 915. 5492. CD₂CD₃
 5493.


5494. H
 5495. H
 5496. H
 5497. CD(CH₃)₂
 916. 5498. CH₂CH₃
 5499. H
 5500. CH₂CH₃
 5501. H
 5502. CH₂CH₃
 5503. CH₂CH₃
 917. 5504. CH₂CH₃
 5505. H
 5506. CH(CH₃)₂
 5507. H
 5508. CH₂CH₃
 5509. CH₂CH₃
 918. 5510. CH₂CH₃
 5511. H
 5512. CH₂CH(CH₃)₂
 5513. H
 5514. CH₂CH₃
 5515. CH₂CH₃
 919. 5516. CH₂CH₃
 5517. H
 5518. C(CH₃)₃
 5519. H
 5520. CH₂CH₃
 5521. CH₂CH₃
 920. 5522. CH₂CH₃
 5523. H
 5524. CH₂C(CH₃)₃
 5525. H
 5526. CH₂CH₃
 5527. CH₂CH₃
 921. 5528. CH₂CH₃
 5529. H
 5530. CH₂CH₂CF₃
 5531. H
 5532. CH₂CH₃
 5533. CH₂CH₃
 922. 5534. CH₂CH₃
 5535. H
 5536. CH₂CCF₃(CH₃)₂
 5537. H
 5538. CH₂CH₃
 5539. CH₂CH₃
 923. 5540. CH₂CH₃
 5541. H
 5542.


5543. H
 5544. CH₂CH₃
 5545. CH₂CH₃
 924. 5546. CH₂CH₃
 5547. H
 5548.


5549. H
 5550. CH₂CH₃
 5551. CH₂CH₃
 925. 5552. CH₂CH₃
 5553. H
 5554.


5555. H
 5556. CH₂CH₃
 5557. CH₂CH₃
 926. 5558. CH₂CH₃
 5559. H
 5560.


5561. H
 5562. CH₂CH₃
 5563. CH₂CH₃
 927. 5564. CH₂CH₃
 5565. H
 5566.


5567. H
 5568. CH₂CH₃
 5569. CH₂CH₃
 928. 5570. CH₂CH₃
 5571. H
 5572.


5573. H
 5574. CH2CH3
 5575. CH2CH3
 929. 5576. CH₂CH₃
 5577. H
 5578.


5579. H
 5580. CH₂CH₃
 5581. CH₂CH₃
 930. 5582. CH₂CH₃
 5583. H
 5584.


5585. H
 5586. CH₂CH₃
 5587. CH₂CH₃
 931. 5588. CH₂CH₃
 5589. H
 5590.


5591. H
 5592. CH₂CH₃
 5593. CH₂CH₃
 932. 5594. CH₂CH₃
 5595. H
 5596.


5597. H
 5598. CH₂CH₃
 5599. CH₂CH₃
 933. 5600. CH₂CH₃
 5601. H
 5602.


5603. H
 5604. CH₂CH₃
 5605. CH₂CH₃
 934. 5606. CH₂CH₃
 5607. H
 5608.


5609. H
 5610. CH₂CH₃
 5611. CH₂CH₃
 935. 5612. CH₂CH₃
 5613. H
 5614.


5615. H
 5616. CH₂CH₃
 5617. CH₂CH₃
 936. 5618. CH₂CH₃
 5619. H
 5620.


5621. H
 5622. CH₂CH₃
 5623. CH₂CH₃
 937. 5624. CH₂CH₃
 5625. H
 5626.


5627. H
 5628. CH₂CH₃
 5629. CH₂CH₃
 938. 5630. CH₂CH₃
 5631. H
 5632.


5633. H
 5634. CH₂CH₃
 5635. CH₂CH₃
 939. 5636. CH₂CH₃
 5637. H
 5638.


5639. H
 5640. CH₂CH₃
 5641. CH₂CH₃
 940. 5642. CH₂CH₃
 5643. H
 5644.


5645. H
 5646. CH₂CH₃
 5647. CH₂CH₃
 941. 5648. CH₂CH₃
 5649. H
 5650.


5651. H
 5652. CH₂CH₃
 5653. CH₂CH₃
 942. 5654. CH₂CH₃
 5655. H
 5656.


5657. H
 5658. CH₂CH₃
 5659. CH₂CH₃
 943. 5660. CD₂CH₃
 5661. H
 5662. CD₃
 5663. H
 5664. CD(CH₃)₂
 5665. CD(CH₃)₂
 944. 5666. CD₂CH₃
 5667. H
 5668. CD₂CD₃
 5669. H
 5670. CD(CH₃)₂
 5671. CD(CH₃)₂
 945. 5672. CD₂CH₃
 5673. H
 5674. CD₂CH₃
 5675. H
 5676. CD(CH₃)₂
 5677. CD(CH₃)₂
 946. 5678. CD₂CH₃
 5679. H
 5680. CD(CD₃)₂
 5681. H
 5682. CD(CH₃)₂
 5683. CD(CH₃)₂
 947. 5684. CD₂CH₃
 5685. H
 5686. CD(CH₃)₂
 5687. H
 5688. CD(CH₃)₂
 5689. CD(CH₃)₂
 948. 5690. CD₂CH₃
 5691. H
 5692. CD₂CD(CD₃)₂
 5693. H
 5694. CD(CH₃)₂
 5695. CD(CH₃)₂
 949. 5696. CD₂CH₃
 5697. H
 5698. CD₂CH(CH₃)₂
 5699. H
 5700. CD(CH₃)₂
 5701. CD(CH₃)₂
 950. 5702. CD₂CH₃
 5703. H
 5704. CD₂C(CD₃)₃
 5705. H
 5706. CD(CH₃)₂
 5707. CD(CH₃)₂
 951. 5708. CD₂CH₃
 5709. H
 5710. CD₂C(CH₃)₃
 5711. H
 5712. CD(CH₃)₂
 5713. CD(CH₃)₂
 952. 5714. CD₂CH₃
 5715. H
 5716. CD₂CD₂CF₃
 5717. H
 5718. CD(CH₃)₂
 5719. CD(CH₃)₂
 953. 5720. CD₂CH₃
 5721. H
 5722. CD₂CH₂CF₃
 5723. H
 5724. CD(CH₃)₂
 5725. CD(CH₃)₂
 954. 5726. CD₂CH₃
 5727. H
 5728. CD₂CCF₃(CH₃)₂
 5729. H
 5730. CD(CH₃)₂
 5731. CD(CH₃)₂
 955. 5732. CD₂CH₃
 5733. H
 5734.


5735. H
 5736. CD(CH₃)₂
 5737. CD(CH₃)₂
 956. 5738. CD₂CH₃
 5739. H
 5740.


5741. H
 5742. CD(CH₃)₂
 5743. CD(CH₃)₂
 957. 5744. CD₂CH₃
 5745. H
 5746.


5747. H
 5748. CD(CH₃)₂
 5749. CD(CH₃)₂
 958. 5750. CD₂CH₃
 5751. H
 5752.

5753 H
 5754. CD(CH₃)₂
 5755. CD(CH₃)₂
 959. 5756. CD₂CH₃
 5757. H
 5758.


5759. H
 5760. CD(CH₃)₂
 5761. CD(CH₃)₂
 960. 5762. CD₂CH₃
 5763. H
 5764.


5765. H
 5766. CD(CH₃)₂
 5767. CD(CH₃)₂
 961. 5768. CD₂CH₃
 5769. H
 5770.


5771. H
 5772. CD(CH₃)₂
 5773. CD(CH₃)₂
 962. 5774. CD₂CH₃
 5775. H
 5776.


5777. H
 5778. CD(CH₃)₂
 5779. CD(CH₃)₂
 963. 5780. CD₂CH₃
 5781. H
 5782.


5783. H
 5784. CD(CH₃)₂
 5785. CD(CH₃)₂
 964. 5786. CD₂CH₃
 5787. H
 5788.


5789. H
 5790. CD(CH₃)₂
 5791. CD(CH₃)₂
 965. 5792. CD₂CH₃
 5793. H
 5794.


5795. H
 5796. CD(CH₃)₂
 5797. CD(CH₃)₂
 966. 5798. CD₂CH₃
 5799. H
 5800.


5801. H
 5802. CD(CH₃)₂
 5803. CD(CH₃)₂
 967. 5804. CD₂CH₃
 5805. H
 5806.


5807. H
 5808. CD(CH₃)₂
 5809. CD(CH₃)₂
 968. 5810. CD₂CH₃
 5811. H
 5812.


5813. H
 5814. CD(CH₃)₂
 5815. CD(CH₃)₂
 969. 5816. CD₂CH₃
 5817. H
 5818.


5819. H
 5820. CD(CH₃)₂
 5821. CD(CH₃)₂
 970. 5822. CD₂CH₃
 5823. H
 5824.


5825. H
 5826. CD(CH₃)₂
 5827. CD(CH₃)₂
 971. 5828. CD₂CH₃
 5829. H
 5830.


5831. H
 5832. CD(CH₃)₂
 5833. CD(CH₃)₂
 972. 5834. CD₂CH₃
 5835. H
 5836.


5837. H
 5838. CD(CH₃)₂
 5839. CD(CH₃)₂
 973. 5840. CD₂CH₃
 5841. H
 5842.


5843. H
 5844. CD(CH₃)₂
 5845. CD(CH₃)₂
 974. 5846. CD₂CH₃
 5847. H
 5848.


5849. H
 5850. CD(CH₃)₂
 5851. CD(CH₃)₂
 975. 5852. CD₂CD₃
 5853. CD₃
 5854. CD₃
 5855. H
 5856. H
 5857. CD₂CD(CD₃)₂
 976. 5858. CD₂CD₃
 5859. CD₃
 5860. CD₂CD₃
 5861. H
 5862. H
 5863. CD₂CD(CD₃)₂
 977. 5864. CD₂CD₃
 5865. CD₃
 5866. CD₂CH₃
 5867. H
 5868. H
 5869. CD₂CD(CD₃)₂
 978. 5870. CD₂CD₃
 5871. CD₃
 5872. CD(CD₃)₂
 5873. H
 5874. H
 5875. CD₂CD(CD₃)₂
 979. 5876. CD₂CD₃
 5877. CD₃
 5878. CD(CH₃)₂
 5879. H
 5880. H
 5881. CD₂CD(CD₃)₂
 980. 5882. CD₂CD₃
 5883. CD₃
 5884. CD₂CD(CD₃)₂
 5885. H
 5886. H
 5887. CD₂CD(CD₃)₂
 981. 5888. CD₂CD₃
 5889. CD₃
 5890. CD₂CH(CH₃)₂
 5891. H
 5892. H
 5893. CD₂CD(CD₃)₂
 982. 5894. CD₂CD₃
 5895. CD₃
 5896. CD₂C(CD₃)₃
 5897. H
 5898. H
 5899. CD₂CD(CD₃)₂
 983. 5900. CD₂CD₃
 5901. CD₃
 5902. CD₂C(CH₃)₃
 5903. H
 5904. H
 5905. CD₂CD(CD₃)₂
 984. 5906. CD₂CD₃
 5907. CD₃
 5908. CD₂CD₂CF₃
 5909. H
 5910. H
 5911. CD₂CD(CD₃)₂
 985. 5912. CD₂CD₃
 5913. CD₃
 5914. CD₂CH₂CF₃
 5915. H
 5916. H
 5917. CD₂CD(CD₃)₂
 986. 5918. CD₂CD₃
 5919. CD₃
 5920. CD₂CCF₃(CH₃)₂
 5921. H
 5922. H
 5923. CD₂CD(CD₃)₂
 987. 5924. CD₂CD₃
 5925. CD₃
 5926.


5927. H
 5928. H
 5929. CD₂CD(CD₃)₂
 988. 5930. CD₂CD₃
 5931. CD₃
 5932.


5933. H
 5934. H
 5935. CD₂CD(CD₃)₂
 989. 5936. CD₂CD₃
 5937. CD₃
 5938.


5939. H
 5940. H
 5941. CD₂CD(CD₃)₂
 990. 5942. CD₂CD₃
 5943. CD₃
 5944.


5945. H
 5946. H
 5947. CD₂CD(CD₃)₂
 991. 5948. CD₂CD₃
 5949. CD₃
 5950.


5951. H
 5952. H
 5953. CD₂CD(CD₃)₂
 992. 5954. CD₂CD₃
 5955. CD₃
 5956.


5957. H
 5958. H
 5959. CD₂CD(CD₃)₂
 993. 5960. CD₂CD₃
 5961. CD₃
 5962.


5963. H
 5964. H
 5965. CD₂CD(CD₃)₂
 994. 5966. CD₂CD₃
 5967. CD₃
 5968.


5969. H
 5970. H
 5971. CD₂CD(CD₃)₂
 995. 5972. CD₂CD₃
 5973. CD₃
 5974.


5975. H
 5976. H
 5977. CD₂CD(CD₃)₂
 996. 5978. CD₂CD₃
 5979. CD₃
 5980.


5981. H
 5982. H
 5983. CD₂CD(CD₃)₂
 997. 5984. CD₂CD₃
 5985. CD₃
 5986.


5987. H
 5988. H
 5989. CD₂CD(CD₃)₂
 998. 5990. CD₂CD₃
 5991. CD₃
 5992.


5993. H
 5994. H
 5995. CD₂CD(CD₃)₂
 999. 5996. CD₂CD₃
 5997. CD₃
 5998.


5999. H
 6000. H
 6001. CD₂CD(CD₃)₂
 1000. 6002. CD₂CD₃
 6003. CD₃
 6004.


6005. H
 6006. H
 6007. CD₂CD(CD₃)₂
 1001. 6008. CD₂CD₃
 6009. CD₃
 6010.


6011. H
 6012. H
 6013. CD₂CD(CD₃)₂
 1002. 6014. CD₂CD₃
 6015. CD₃
 6016.


6017. H
 6018. H
 6019. CD₂CD(CD₃)₂
 1003. 6020. CD₂CD₃
 6021. CD₃
 6022.


6023. H
 6024. H
 6025. CD₂CD(CD₃)₂
 1004. 6026. CD₂CD₃
 6027. CD₃
 6028.


6029. H
 6030. H
 6031. CD₂CD(CD₃)₂
 1005. 6032. CD₂CD₃
 6033. CD₃
 6034.


6035. H
 6036. H
 6037. CD₂CD(CD₃)₂
 1006. 6038. CD₂CD₃
 6039. CD₃
 6040.


6041. H
 6042. H
 6043. CD₂CD(CD₃)₂
 1007. 6044. CD₂CH₃
 6045. H
 6046. H
 6047. CD₃
 6048. CD₂CH₃
 6049. CD₂CH₃
 1008. 6050. CD₂CH₃
 6051. H
 6052. H
 6053. CD₂CD₃
 6054. CD₂CH₃
 6055. CD₂CH₃
 1009. 6056. CD₂CH₃
 6057. H
 6058. H
 6059. CD₂CH₃
 6060. CD₂CH₃
 6061. CD₂CH₃
 1010. 6062. CD₂CH₃
 6063. H
 6064. H
 6065. CD(CD₃)₂
 6066. CD₂CH₃
 6067. CD₂CH₃
 1011. 6068. CD₂CH₃
 6069. H
 6070. H
 6071. CD(CH₃)₂
 6072. CD₂CH₃
 6073. CD₂CH₃
 1012. 6074. CD₂CH₃
 6075. H
 6076. H
 6077. CD₂CD(CD₃)₂
 6078. CD₂CH₃
 6079. CD₂CH₃
 1013. 6080. CD₂CH₃
 6081. H
 6082. H
 6083. CD₂CH(CH₃)₂
 6084. CD₂CH₃
 6085. CD₂CH₃
 1014. 6086. CD₂CH₃
 6087. H
 6088. H
 6089. CD₂C(CD₃)₃
 6090. CD₂CH₃
 6091. CD₂CH₃
 1015. 6092. CD₂CH₃
 6093. H
 6094. H
 6095. CD₂C(CH₃)₃
 6096. CD₂CH₃
 6097. CD₂CH₃
 1016. 6098. CD₂CH₃
 6099. H
 6100. H
 6101. CD₂CD₂CF₃
 6102. CD₂CH₃
 6103. CD₂CH₃
 1017. 6104. CD₂CH₃
 6105. H
 6106. H
 6107. CD₂CH₂CF₃
 6108. CD₂CH₃
 6109. CD₂CH₃
 1018. 6110. CD₂CH₃
 6111. H
 6112. H
 6113. CD₂CCF₃(CH₃)₂
 6114. CD₂CH₃
 6115. CD₂CH₃
 1019. 6116. CD₂CH₃
 6117. H
 6118. H
 6119.


6120. CD₂CH₃
 6121. CD₂CH₃
 1020. 6122. CD₂CH₃
 6123. H
 6124. H
 6125.


6126. CD₂CH₃
 6127. CD₂CH₃
 1021. 6128. CD₂CH₃
 6129. H
 6130. H 6131


6132. CD₂CH₃
 6133. CD₂CH₃
 1022. 6134. CD₂CH₃
 6135. H
 6136. H 6137


6138. CD₂CH₃
 6139. CD₂CH₃
 1023. 6140. CD₂CH₃
 6141. H
 6142. H
 6143.


6144. CD₂CH₃
 6145. CD₂CH₃
 1024. 6146. CD₂CH₃
 6147. H
 6148. H 6149


6150. CD₂CH₃
 6151. CD₂CH₃
 1025. 6152. CD₂CH₃
 6153. H
 6154. H
 6155.


6156. CD₂CH₃
 6157. CD₂CH₃
 1026. 6158. CD₂CH₃
 6159. H
 6160. H
 6161.


6162. CD₂CH₃
 6163. CD₂CH₃
 1027. 6164. CD₂CH₃
 6165. H
 6166. H
 6167.


6168. CD₂CH₃
 6169. CD₂CH₃
 1028. 6170. CD₂CH₃
 6171. H
 6172. H
 6173.


6174. CD₂CH₃
 6175. CD₂CH₃
 1029. 6176. CD₂CH₃
 6177. H
 6178. H
 6179.


6180. CD₂CH₃
 6181. CD₂CH₃
 1030. 6182. CD₂CH₃
 6183. H
 6184. H
 6185.


6186. CD₂CH₃
 6187. CD₂CH₃
 1031. 6188. CD₂CH₃
 6189. H
 6190. H
 6191.


6192. CD₂CH₃
 6193. CD₂CH₃
 1032. 6194. CD₂CH₃
 6195. H
 6196. H
 6197.


6198. CD₂CH₃
 6199. CD₂CH₃
 1033. 6200. CD₂CH₃
 6201. H
 6202. H
 6203.


6204. CD₂CH₃
 6205. CD₂CH₃
 1034. 6206. CD₂CH₃
 6207. H
 6208. H
 6209.


6210. CD₂CH₃
 6211. CD₂CH₃
 1035. 6212. CD₂CH₃
 6213. CD3
 6214. H
 6215. CD₃
 6216. CD(CH₃)₂
 6217. CD(CH₃)₂
 1036. 6218. CD₂CH₃
 6219. CD3
 6220. H
 6221. CD₂CD₃
 6222. CD(CH₃)₂
 6223. CD(CH₃)₂
 1037. 6224. CD₂CH₃
 6225. CD3
 6226. H
 6227. CD₂CH₃
 6228. CD(CH₃)₂
 6229. CD(CH₃)₂
 1038. 6230. CD₂CH₃
 6231. CD3
 6232. H
 6233. CD(CD₃)₂
 6234. CD(CH₃)₂
 6235. CD(CH₃)₂
 1039. 6236. CD₂CH₃
 6237. CD3
 6238. H
 6239. CD(CH₃)₂
 6240. CD(CH₃)₂
 6241. CD(CH₃)₂
 1040. 6242. CD₂CH₃
 6243. CD3
 6244. H
 6245. CD₂CD(CD₃)₂
 6246. CD(CH₃)₂
 6247. CD(CH₃)₂
 1041. 6248. CD₂CH₃
 6249. CD₃
 6250. H
 6251. CD₂CH(CH₃)₂
 6252. CD(CH₃)₂
 6253. CD(CH₃)₂
 1042. 6254. CD₂CH₃
 6255. CD₃
 6256. H
 6257. CD₂C(CD₃)₃
 6258. CD(CH₃)₂
 6259. CD(CH₃)₂
 1043. 6260. CD₂CH₃
 6261. CD₃
 6262. H
 6263. CD₂C(CH₃)₃
 6264. CD(CH₃)₂
 6265. CD(CH₃)₂
 1044. 6266. CD₂CH₃
 6267. CD₃
 6268. H
 6269. CD₂CD₂CF₃
 6270. CD(CH₃)₂
 6271. CD(CH₃)₂
 1045. 6272. CD₂CH₃
 6273. CD₃
 6274. H
 6275. CD₂CH₂CF₃
 6276. CD(CH₃)₂
 6277. CD(CH₃)₂
 1046. 6278. CD₂CH₃
 6279. CD₃
 6280. H
 6281. CD₂CCF₃(CH₃)₂
 6282. CD(CH₃)₂
 6283. CD(CH₃)₂
 1047. 6284. CD₂CH₃
 6285. CD₃
 6286. H
 6287.


6288. CD(CH₃)₂
 6289. CD(CH₃)₂
 1048. 6290. CD₂CH₃
 6291. CD₃
 6292. H
 6293.


6294. CD(CH₃)₂
 6295. CD(CH₃)₂
 1049. 6296. CD₂CH₃
 6297. CD₃
 6298. H
 6299.


6300. CD(CH₃)₂
 6301. CD(CH₃)₂
 1050. 6302. CD₂CH₃
 6303. CD₃
 6304. H
 6305.


6306. CD(CH₃)₂
 6307. CD(CH₃)₂
 1051. 6308. CD₂CH₃
 6309. CD₃
 6310. H
 6311.


6312. CD(CH₃)₂
 6313. CD(CH₃)₂
 1052. 6314. CD₂CH₃
 6315. CD₃
 6316. H
 6317.


6318. CD(CH₃)₂
 6319. CD(CH₃)₂
 1053. 6320. CD₂CH₃
 6321. CD₃
 6322. H
 6323.


6324. CD(CH₃)₂
 6325. CD(CH₃)₂
 1054. 6326. CD₂CH₃
 6327. CD₃
 6328. H
 6329.


6330. CD(CH₃)₂
 6331. CD(CH₃)₂
 1055. 6332. CD₂CH₃
 6333. CD₃
 6334. H
 6335.


6336. CD(CH₃)₂
 6337. CD(CH₃)₂
 1056. 6338. CD₂CH₃
 6339. CD₃
 6340. H
 6341.


6342. CD(CH₃)₂
 6343. CD(CH₃)₂
 1057. 6344. CD₂CH₃
 6345. CD₃
 6346. H
 6347.


6348. CD(CH₃)₂
 6349. CD(CH₃)₂
 1058. 6350. CD₂CH₃
 6351. CD₃
 6352. H
 6353.


6354. CD(CH₃)₂
 6355. CD(CH₃)₂
 1059. 6356. CD₂CH₃
 6357. CD₃
 6358. H
 6359.


6360. CD(CH₃)₂
 6361. CD(CH₃)₂
 1060. 6362. CD₂CH₃
 6363. CD₃
 6364. H
 6365.


6366. CD(CH₃)₂
 6367. CD(CH₃)₂
 1061. 6368. CD₂CH₃
 6369. CD₃
 6370. H
 6371.


6372. CD(CH₃)₂
 6373. CD(CH₃)₂
 1062. 6374. CD₂CH₃
 6375. CD₃
 6376. H
 6377.


6378. CD(CH₃)₂
 6379. CD(CH₃)₂
 1063. 6380. CD₂CH₃
 6381. CD₃
 6382. H
 6383.


6384. CD(CH₃)₂
 6385. CD(CH₃)₂
 1064. 6386. CD₂CH₃
 6387. CD₃
 6388. H
 6389.


6390. CD(CH₃)₂
 6391. CD(CH₃)₂
 1065. 6392. CD₂CH₃
 6393. CD₃
 6394. H 6395


6396. CD(CH₃)₂
 6397. CD(CH₃)₂
 1066. 6398. CD₂CH₃
 6399. CD₃
 6400. H
 6401.


6402. CD(CH₃)₂
 6403. CD(CH₃)₂
 1067. 6404. CD(CH₃)₂
 6405. CD₃
 6406. H
 6407. H
 6408. H
 6409.


1068. 6410. CD(CH₃)₂
 6411. CD₂CD₃
 6412. H
 6413. H
 6414. H
 6415.


1069. 6416. CD(CH₃)₂
 6417. CD₂CH₃
 6418. H
 6419. H
 6420. H
 6421.


1070. 6422. CD(CH₃)₂
 6423. CD(CD₃)₂
 6424. H
 6425. H
 6426. H
 6427.


1071. 6428. CD(CH₃)₂
 6429. CD(CH₃)₂
 6430. H
 6431. H
 6432. H
 6433.


1072. 6434. CD(CH₃)₂
 6435. CD₂CD(CD₃)₂
 6436. H
 6437. H
 6438. H
 6439.


1073. 6440. CD(CH₃)₂
 6441. CD₂CH(CH₃)₂
 6442. H
 6443. H
 6444. H
 6445.


1074. 6446. CD(CH₃)₂
 6447. CD₂C(CD₃)₃
 6448. H
 6449. H
 6450. H
 6451.


1075. 6452. CD(CH₃)₂
 6453. CD₂C(CH₃)₃
 6454. H
 6455. H
 6456. H
 6457.


1076. 6458. CD(CH₃)₂
 6459. CD₂CD₂C
 6460. H
 6461. H
 6462. H
 6463.


1077. 6464. CD(CH₃)₂
 6465. CD₂CH₂CF₃
 6466. H
 6467. H
 6468. H
 6469.


1078. 6470. CD(CH₃)₂
 6471. CD₂CCF₃(CH₃)₂
 6472. H
 6473. H
 6474. H
 6475.


1079. 6476. CD(CH₃)₂
 6477.


6478. H
 6479. H
 6480. H
 6481.


1080. 6482. CD(CH₃)₂
 6483.


6484. H
 6485. H
 6486. H
 6487.


1081. 6488. CD(CH₃)₂
 6489.


6490. H
 6491. H
 6492. H
 6493.


1082. 6494. CD(CH₃)₂
 6495.


6496. H
 6497. H
 6498. H
 6499.


1083. 6500. CD(CH₃)₂
 6501.


6502. H
 6503. H
 6504. H
 6505.


1084. 6506. CD(CH₃)₂
 6507.


6508. H
 6509. H
 6510. H
 6511.


1085. 6512. CD(CH₃)₂
 6513.


6514. H
 6515. H
 6516. H
 6517.


1086. 6518. CD(CH₃)₂
 6519.


6520. H
 6521. H
 6522. H
 6523.


1087. 6524. CD(CH₃)₂
 6525.


6526. H
 6527. H
 6528. H
 6529.


1088. 6530. CD(CH₃)₂
 6531.


6532. H
 6533. H
 6534. H
 6535.


1089. 6536. CD(CH₃)₂
 6537.


6538. H
 6539. H
 6540. H
 6541.


1090. 6542. CD(CH₃)₂
 6543.


6544. H
 6545. H
 6546. H
 6547.


1091. 6548. CD(CH₃)₂
 6549.


6550. H
 6551. H
 6552. H
 6553.


1092. 6554. CD(CH₃)₂
 6555.


6556. H
 6557. H
 6558. H
 6559.


1093. 6560. CD(CH₃)₂
 6561.


6562. H
 6563. H
 6564. H
 6565.


1094. 6566. CD(CH₃)₂
 6567.


6568. H
 6569. H
 6570. H
 6571.


1095. 6572. CD(CH₃)₂
 6573.


6574. H
 6575. H
 6576. H
 6577.


1096. 6578. CD(CH₃)₂
 6579.


6580. H
 6581. H
 6582. H
 6583.


1097. 6584. CD(CH₃)₂
 6585.


6586. H
 6587. H
 6588. H
 6589.


1098. 6590. CD(CH₃)₂
 6591.


6592. H
 6593. H
 6594. H
 6595.


1099. 6596. CD(CD₃)₂
 6597. CD₃
 6598. H
 6599. H
 6600. H
 6601.


1100. 6602. CD(CD₃)₂
 6603. CD₂CD₃
 6604. H
 6605. H
 6606. H
 6607.


1101. 6608. CD(CD₃)₂
 6609. CD₂CH₃
 6610. H
 6611. H
 6612. H
 6613.


1102. 6614. CD(CD₃)₂
 6615. CD(CD₃)₂
 6616. H
 6617. H
 6618. H
 6619.


1103. 6620. CD(CD₃)₂
 6621. CD(CH₃)₂
 6622. H
 6623. H
 6624. H
 6625.


1104. 6626. CD(CD₃)₂
 6627. CD₂CD(CD₃)₂
 6628. H
 6629. H
 6630. H
 6631.


1105. 6632. CD(CD₃)₂
 6633. CD₂CH(CH₃)₂
 6634. H
 6635. H
 6636. H
 6637.


1106. 6638. CD(CD₃)₂
 6639. CD₂C(CD₃)₃
 6640. H
 6641. H
 6642. H
 6643.


1107. 6644. CD(CD₃)₂
 6645. CD₂C(CH₃)₃
 6646. H
 6647. H
 6648. H
 6649.


1108. 6650. CD(CD₃)₂
 6651. CD₂CD₂CF₃
 6652. H
 6653. H
 6654. H
 6655.


1109. 6656. CD(CD₃)₂
 6657. CD₂CH₂CF₃
 6658. H
 6659. H
 6660. H
 6661.


1110. 6662. CD(CD₃)₂
 6663. CD₂CCF₃(CH₃)₂
 6664. H
 6665. H
 6666. H
 6667.


1111. 6668. CD(CD₃)₂
 6669.


6670. H
 6671. H
 6672. H
 6673.


1112. 6674. CD(CD₃)₂
 6675.


6676. H
 6677. H
 6678. H
 6679.


1113. 6680. CD(CD₃)₂
 6681.


6682. H
 6683. H
 6684. H
 6685.


1114. 6686. CD(CD₃)₂
 6687.


6688. H
 6689. H
 6690. H
 6691.


1115. 6692. CD(CD₃)₂
 6693.


6694. H
 6695. H
 6696. H
 6697.


1116. 6698. CD(CD₃)₂
 6699.


6700. H
 6701. H
 6702. H
 6703.


1117. 6704. CD(CD₃)₂
 6705.


6706. H
 6707. H
 6708. H
 6709.


1118. 6710. CD(CD₃)₂
 6711.


6712. H
 6713. H
 6714. H
 6715.


1119. 6716. CD(CD₃)₂
 6717.


6718. H
 6719. H
 6720. H
 6721.


1120. 6722. CD(CD₃)₂
 6723.


6724. H
 6725. H
 6726. H
 6727.


1121. 6728. CD(CD₃)₂
 6729.


6730. H
 6731. H
 6732. H
 6733.


1122. 6734. CD(CD₃)₂
 6735.


6736. H
 6737. H
 6738. H
 6739.


1123. 6740. CD(CD₃)₂
 6741.


6742. H
 6743. H
 6744. H
 6745.


1124. 6746. CD(CD₃)₂
 6747.


6748. H
 6749. H
 6750. H
 6751.


1125. 6752. CD(CD₃)₂
 6753.


6754. H
 6755. H
 6756. H
 6757.


1126. 6758. CD(CD₃)₂
 6759.


6760. H
 6761. H
 6762. H
 6763.


1127. 6764. CD(CD₃)₂
 6765.


6766. H
 6767. H
 6768. H
 6769.


1128. 6770. CD(CD₃)₂
 6771.


6772. H
 6773. H
 6774. H
 6775.


1129. 6776. CD(CD₃)₂
 6777.


6778. H
 6779. H
 6780. H
 6781.


1130. 6782. CD(CD₃)₂
 6783.


6784. H
 6785. H
 6786. H
 6787.


1131. 6788. CH(CH₃)₂
 6789. H
 6790. CH₂CH₃
 6791. H
 6792. H
 6793.


1132. 6794. CH(CH₃)₂
 6795. H
 6796. CH(CH₃)₂
 6797. H
 6798. H
 6799.


1133. 6800. CH(CH₃)₂
 6801. H
 6802. CH₂CH(CH₃)₂
 6803. H
 6804. H
 6805.


1134. 6806. CH(CH₃)₂
 6807. H
 6808. C(CH₃)₃
 6809. H
 6810. H
 6811.


1135. 6812. CH(CH₃)₂
 6813. H
 6814. CH₂C(CH₃)₃
 6815. H
 6816. H
 6817.


1136. 6818. CH(CH₃)₂
 6819. H
 6820. CH₂CH₂CF₃
 6821. H
 6822. H
 6823.


1137. 6824. CH(CH₃)₂
 6825. H
 6826. CH₂CCF₃(CH₃)₂
 6827. H
 6828. H
 6829.


1138. 6830. CH(CH₃)₂
 6831. H
 6832.


6833. H
 6834. H
 6835.


1139. 6836. CH(CH₃)₂
 6837. H
 6838.


6839. H
 6840. H
 6841.


1140. 6842. CH(CH₃)₂
 6843. H
 6844.


6845. H
 6846. H
 6847.


1141. 6848. CH(CH₃)₂
 6849. H
 6850.


6851. H
 6852. H
 6853.


1142. 6854. CH(CH₃)₂
 6855. H
 6856.


6857. H
 6858. H
 6859.


1143. 6860. CH(CH₃)₂
 6861. H
 6862.


6863. H
 6864. H
 6865.


1144. 6866. CH(CH₃)₂
 6867. H
 6868.


6869. H
 6870. H
 6871.


1145. 6872. CH(CH₃)₂
 6873. H
 6874.


6875. H
 6876. H
 6877.


1146. 6878. CH(CH₃)₂
 6879. H
 6880.


6881. H
 6882. H
 6883.


1147. 6884. CH(CH₃)₂
 6885. H
 6886.


6887. H
 6888. H
 6889.


1148. 6890. CH(CH₃)₂
 6891. H
 6892.


6893. H
 6894. H
 6895.


1149. 6896. CH(CH₃)₂
 6897. H
 6898.


6899. H
 6900. H
 6901.


1150. 6902. CH(CH₃)₂
 6903. H
 6904.


6905. H
 6906. H
 6907.


1151. 6908. CH(CH₃)₂
 6909. H
 6910.


6911. H
 6912. H
 6913.


1152. 6914. CH(CH₃)₂
 6915. H
 6916.


6917. H
 6918. H
 6919.


1153. 6920. CH(CH₃)₂
 6921. H
 6922.


6923. H
 6924. H
 6925.


1154. 6926. CH(CH₃)₂
 6927. H
 6928.


6929. H
 6930. H
 6931.


1155. 6932. CH(CH₃)₂
 6933. H
 6934.


6935. H
 6936. H
 6937.


1156. 6938. CH(CH₃)₂
 6939. H
 6940.


6941. H
 6942. H
 6943.


1157. 6944. CH(CH₃)₂
 6945. H
 6946.


6947. H
 6948. H
 6949.


1158. 6950. CD(CH₃)₂
 6951. H
 6952. CD₃
 6953. H
 6954.


6955. CD₃
 1159. 6956. CD(CH₃)₂
 6957. H
 6958. CD₂CD₃
 6959. H
 6960.


6961. CD₃
 1160. 6962. CD(CH₃)₂
 6963. H
 6964. CD₂CH₃
 6965. H
 6966.


6967. CD₃
 1161. 6968. CD(CH₃)₂
 6969. H
 6970. CD(CD₃)₂
 6971. H
 6972.


6973. CD₃
 1162. 6974. CD(CH₃)₂
 6975. H
 6976. CD(CH₃)₂
 6977. H
 6978.


6979. CD₃
 1163. 6980. CD(CH₃)₂
 6981. H
 6982. CD₂CD(CD₃)₂
 6983. H
 6984.


6985. CD₃
 1164. 6986. CD(CH₃)₂
 6987. H
 6988. CD₂CH(CH₃)₂
 6989. H
 6990.


6991. CD₃
 1165. 6992. CD(CH₃)₂
 6993. H
 6994. CD₂C(CD₃)₃
 6995. H
 6996.


6997. CD₃
 1166. 6998. CD(CH₃)₂
 6999. H
 7000. CD₂C(CH₃)₃
 7001. H
 7002.


7003. CD₃
 1167. 7004. CD(CH₃)₂
 7005. H
 7006. CD₂CD₂CF₃
 7007. H
 7008.


7009. CD₃
 1168. 7010. CD(CH₃)₂
 7011. H
 7012. CD₂CH₂CF₃
 7013. H
 7014.


7015. CD₃
 1169. 7016. CD(CH₃)₂
 7017. H
 7018. CD₂CCF₃(CH₃)₂
 7019. H
 7020.


7021. CD₃
 1170. 7022. CD(CH₃)₂
 7023. H
 7024.


7025. H
 7026.


7027. CD₃
 1171. 7028. CD(CH₃)₂
 7029. H
 7030.


7031. H
 7032.


7033. CD₃
 1172. 7034. CD(CH₃)₂
 7035. H
 7036.


7037. H
 7038.


7039. CD₃
 1173. 7040. CD(CH₃)₂
 7041. H
 7042.

7043 H
 7044.


7045. CD₃
 1174. 7046. CD(CH₃)₂
 7047. H
 7048.


7049. H
 7050.


7051. CD₃
 1175. 7052. CD(CH₃)₂
 7053. H
 7054.


7055. H
 7056.


7057. CD₃
 1176. 7058. CD(CH₃)₂
 7059. H
 7060.


7061. H
 7062.


7063. CD₃
 1177. 7064. CD(CH₃)₂
 7065. H
 7066.


7067. H
 7068.


7069. CD₃
 1178. 7070. CD(CH₃)₂
 7071. H
 7072.


7073. H
 7074.


7075. CD₃
 1179. 7076. CD(CH₃)₂
 7077. H
 7078.


7079. H
 7080.


7081. CD₃
 1180. 7082. CD(CH₃)₂
 7083. H
 7084.


7085. H
 7086.


7087. CD₃
 1181. 7088. CD(CH₃)₂
 7089. H
 7090.


7091. H
 7092.


7093. CD₃
 1182. 7094. CD(CH₃)₂
 7095. H
 7096.


7097. H
 7098.


7099. CD₃
 1183. 7100. CD(CH₃)₂
 7101. H
 7102.


7103. H
 7104.


7105. CD₃
 1184. 7106. CD(CH₃)₂
 7107. H
 7108.


7109. H
 7110.


7111. CD₃
 1185. 7112. CD(CH₃)₂
 7113. H
 7114.


7115. H
 7116.


7117. CD₃
 1186. 7118. CD(CH₃)₂
 7119. H
 7120.


7121. H
 7122.


7123. CD₃
 1187. 7124. CD(CH₃)₂
 7125. H
 7126.


7127. H
 7128.


7129. CD₃
 1188. 7130. CD(CH₃)₂
 7131. H
 7132.


7133. H
 7134.


7135. CD₃
 1189. 7136. CD(CH₃)₂
 7137. H
 7138.


7139. H
 7140.


7141. CD₃
 1190. 7142. CD(CD₃)₂
 7143. H
 7144. CD₃
 7145. H
 7146. CD(CD₃)₂
 7147. CD(CD₃)₂
 1191. 7148. CD(CD₃)₂
 7149. H
 7150. CD₂CD₃
 7151. H
 7152. CD(CD₃)₂
 7153. CD(CD₃)₂
 1192. 7154. CD(CD₃)₂
 7155. H
 7156. CD₂CH₃
 7157. H
 7158. CD(CD₃)₂
 7159. CD(CD₃)₂
 1193. 7160. CD(CD₃)₂
 7161. H
 7162. CD(CD₃)₂
 7163. H
 7164. CD(CD₃)₂
 7165. CD(CD₃)₂
 1194. 7166. CD(CD₃)₂
 7167. H
 7168. CD(CH₃)₂
 7169. H
 7170. CD(CD₃)₂
 7171. CD(CD₃)₂
 1195. 7172. CD(CD₃)₂
 7173. H
 7174. CD₂CD(CD₃)₂
 7175. H
 7176. CD(CD₃)₂
 7177. CD(CD₃)₂
 1196. 7178. CD(CD₃)₂
 7179. H
 7180. CD₂CH(CH₃)₂
 7181. H
 7182. CD(CD₃)₂
 7183. CD(CD₃)₂
 1197. 7184. CD(CD₃)₂
 7185. H
 7186. CD₂C(CD₃)₃
 7187. H
 7188. CD(CD₃)₂
 7189. CD(CD₃)₂
 1198. 7190. CD(CD₃)₂
 7191. H
 7192. CD₂C(CH₃)₃
 7193. H
 7194. CD(CD₃)₂
 7195. CD(CD₃)₂
 1199. 7196. CD(CD₃)₂
 7197. H
 7198. CD₂CD₂CF₃
 7199. H
 7200. CD(CD₃)₂
 7201. CD(CD₃)₂
 1200. 7202. CD(CD₃)₂
 7203. H
 7204. CD₂CH₂CF₃
 7205. H
 7206. CD(CD₃)₂
 7207. CD(CD₃)₂
 1201. 7208. CD(CD₃)₂
 7209. H
 7210. CD₂CCF₃(CH₃)₂
 7211. H
 7212. CD(CD₃)₂
 7213. CD(CD₃)₂
 1202. 7214. CD(CD₃)₂
 7215. H
 7216.


7217. H
 7218. CD(CD₃)₂
 7219. CD(CD₃)₂
 1203. 7220. CD(CD₃)₂
 7221. H
 7222.


7223. H
 7224. CD(CD₃)₂
 7225. CD(CD₃)₂
 1204. 7226. CD(CD₃)₂
 7227. H
 7228.


7229. H
 7230. CD(CD₃)₂
 7231. CD(CD₃)₂
 1205. 7232. CD(CD₃)₂
 7233. H
 7234.


7235. H
 7236. CD(CD₃)₂
 7237. CD(CD₃)₂
 1206. 7238. CD(CD₃)₂
 7239. H
 7240.


7241. H
 7242. CD(CD₃)₂
 7243. CD(CD₃)₂
 1207. 7244. CD(CD₃)₂
 7245. H
 7246.


7247. H
 7248. CD(CD₃)₂
 7249. CD(CD₃)₂
 1208. 7250. CD(CD₃)₂
 7251. H
 7252.


7253. H
 7254. CD(CD₃)₂
 7255. CD(CD₃)₂
 1209. 7256. CD(CD₃)₂
 7257. H
 7258.


7259. H
 7260. CD(CD₃)₂
 7261. CD(CD₃)₂
 1210. 7262. CD(CD₃)₂
 7263. H
 7264.


7265. H
 7266. CD(CD₃)₂
 7267. CD(CD₃)₂
 1211. 7268. CD(CD₃)₂
 7269. H
 7270.


7271. H
 7272. CD(CD₃)₂
 7273. CD(CD₃)₂
 1212. 7274. CD(CD₃)₂
 7275. H
 7276.


7277. H
 7278. CD(CD₃)₂
 7279. CD(CD₃)₂
 1213. 7280. CD(CD₃)₂
 7281. H
 7282.


7283. H
 7284. CD(CD₃)₂
 7285. CD(CD₃)₂
 1214. 7286. CD(CD₃)₂
 7287. H
 7288.


7289. H
 7290. CD(CD₃)₂
 7291. CD(CD₃)₂
 1215. 7292. CD(CD₃)₂
 7293. H
 7294.


7295. H
 7296. CD(CD₃)₂
 7297. CD(CD₃)₂
 1216. 7298. CD(CD₃)₂
 7299. H
 7300.


7301. H
 7302. CD(CD₃)₂
 7303. CD(CD₃)₂
 1217. 7304. CD(CD₃)₂
 7305. H
 7306.


7307. H
 7308. CD(CD₃)₂
 7309. CD(CD₃)₂
 1218. 7310. CD(CD₃)₂
 7311. H
 7312.


7313. H
 7314. CD(CD₃)₂
 7315. CD(CD₃)₂
 1219. 7316. CD(CD₃)₂
 7317. H
 7318.


7319. H
 7320. CD(CD₃)₂
 7321. CD(CD₃)₂
 1220. 7322. CD(CD₃)₂
 7323. H 7324


7325. H
 7326. CD(CD₃)₂
 7327. CD(CD₃)₂
 1221. 7328. CD(CD₃)₂
 7329. H
 7330.


7331. H
 7332. CD(CD₃)₂
 7333. CD(CD₃)₂
 1222. 7334. CH(CH₃)₂
 7335. H
 7336. H
 7337. CH₃
 7338. H
 7339. CH₃
 1223. 7340. CH(CH₃)₂
 7341. H
 7342. H
 7343. CH₂CH₃
 7344. H
 7345. CH₃
 1224. 7346. CH(CH₃)₂
 7347. H
 7348. H
 7349. CH(CH₃)₂
 7350. H
 7351. CH₃
 1225. 7352. CH(CH₃)₂
 7353. H
 7354. H
 7355. CH₂CH(CH₃)₂
 7356. H
 7357. CH₃
 1226. 7358. CH(CH₃)₂
 7359. H
 7360. H
 7361. C(CH₃)₃
 7362. H
 7363. CH₃
 1227. 7364. CH(CH₃)₂
 7365. H
 7366. H
 7367. CH₂C(CH₃)₃
 7368. H
 7369. CH₃
 1228. 7370. CH(CH₃)₂
 7371. H
 7372. H
 7373. CH₂CH₂CF₃
 7374. H
 7375. CH₃
 1229. 7376. CH(CH₃)₂
 7377. H
 7378. H
 7379. CH₂CCF₃(CH₃)₂
 7380. H
 7381. CH₃
 1230. 7382. CH(CH₃)₂
 7383. H
 7384. H
 7385.


7386. H
 7387. CH₃
 1231. 7388. CH(CH₃)₂
 7389. H
 7390. H
 7391.


7392. H
 7393. CH₃
 1232. 7394. CH(CH₃)₂
 7395. H
 7396. H
 7397.


7398. H
 7399. CH₃
 1233. 7400. CH(CH₃)₂
 7401. H
 7402. H 7403


7404. H
 7405. CH₃
 1234. 7406. CH(CH₃)₂
 7407. H
 7408. H
 7409.


7410. H
 7411. CH₃
 1235. 7412. CH(CH₃)₂
 7413. H
 7414. H
 7415.


7416. H
 7417. CH₃
 1236. 7418. CH(CH₃)₂
 7419. H
 7420. H
 7421.


7422. H
 7423. CH₃
 1237. 7424. CH(CH₃)₂
 7425. H
 7426. H
 7427.


7428. H
 7429. CH₃
 1238. 7430. CH(CH₃)₂
 7431. H
 7432. H
 7433.


7434. H
 7435. CH₃
 1239. 7436. CH(CH₃)₂
 7437. H
 7438. H
 7439.


7440. H
 7441. CH₃
 1240. 7442. CH(CH₃)₂
 7443. H
 7444. H
 7445.


7446. H
 7447. CH₃
 1241. 7448. CH(CH₃)₂
 7449. H
 7450. H
 7451.


7452. H
 7453. CH₃
 1242. 7454. CH(CH₃)₂
 7455. H
 7456. H
 7457.


7458. H
 7459. CH₃
 1243. 7460. CH(CH₃)₂
 7461. H
 7462. H
 7463.


7464. H
 7465. CH₃
 1244. 7466. CH(CH₃)₂
 7467. H
 7468. H
 7469.


7470. H
 7471. CH₃
 1245. 7472. CH(CH₃)₂
 7473. H
 7474. H
 7475.


7476. H
 7477. CH₃
 1246. 7478. CH(CH₃)₂
 7479. H
 7480. H
 7481.


7482. H
 7483. CH₃
 1247. 7484. CH(CH₃)₂
 7485. H
 7486. H
 7487.


7488. H
 7489. CH₃
 1248. 7490. CH(CH₃)₂
 7491. H
 7492. H
 7493.


7494. H
 7495. CH₃
 1249. 7496. CH(CH₃)₂
 7497. H
 7498. H
 7499.


7500. H
 7501. CH₃
 1250. 7502. CH(CH₃)₂
 7503. CH₃
 7504. CH3
 7505. H
 7506. CH₃
 7507. CH₃
 1251. 7508. CH(CH₃)₂
 7509. CH₂CH₃
 7510. CH3
 7511. H
 7512. CH₃
 7513. CH₃
 1252. 7514. CH(CH₃)₂
 7515. CH(CH₃)₂
 7516. CH3
 7517. H
 7518. CH₃
 7519. CH₃
 1253. 7520. CH(CH₃)₂
 7521. CH₂CH(CH₃)₂
 7522. CH3
 7523. H
 7524. CH₃
 7525. CH₃
 1254. 7526. CH(CH₃)₂
 7527. C(CH₃)₃
 7528. CH₃
 7529. H
 7530. CH₃
 7531. CH₃
 1255. 7532. CH(CH₃)₂
 7533. CH₂C(CH₃)₃
 7534. CH₃
 7535. H
 7536. CH₃
 7537. CH₃
 1256. 7538. CH(CH₃)₂
 7539. CH₂CH₂CF₃
 7540. CH₃
 7541. H
 7542. CH₃
 7543. CH₃
 1257. 7544. CH(CH₃)₂
 7545. CH₂CCF₃(CH₃)₂
 7546. CH₃
 7547. H
 7548. CH₃
 7549. CH₃
 1258. 7550. CH(CH₃)₂
 7551.


7552. CH₃
 7553. H
 7554. CH₃
 7555. CH₃
 1259. 7556. CH(CH₃)₂
 7557.


7558. CH₃
 7559. H
 7560. CH₃
 7561. CH₃
 1260. 7562. CH(CH₃)₂
 7563.


7564. CH₃
 7565. H
 7566. CH₃
 7567. CH₃
 1261. 7568. CH(CH₃)₂
 7569.


7570. CH₃
 7571. H
 7572. CH₃
 7573. CH₃
 1262. 7574. CH(CH₃)₂
 7575.


7576. CH₃
 7577. H
 7578. CH₃
 7579. CH₃
 1263. 7580. CH(CH₃)₂ 7581 .


7582. CH₃
 7583. H
 7584. CH₃
 7585. CH₃
 1264. 7586. CH(CH₃)₂
 7587.


7588. CH₃
 7589. H
 7590. CH₃
 7591. CH₃
 1265. 7592. CH(CH₃)₂
 7593.


7594. CH₃
 7595. H
 7596. CH₃
 7597. CH₃
 1266. 7598. CH(CH₃)₂
 7599.


7600. CH₃
 7601. H
 7602. CH₃
 7603. CH₃
 1267. 7604. CH(CH₃)₂
 7605.


7606. CH₃
 7607. H
 7608. CH₃
 7609. CH₃
 1268. 7610. CH(CH₃)₂ 7611 .


7612. CH₃
 7613. H
 7614. CH₃
 7615. CH₃
 1269. 7616. CH(CH₃)₂
 7617.


7618. CH₃
 7619. H
 7620. CH₃
 7621. CH₃
 1270. 7622. CH(CH₃)₂
 7623.


7624. CH₃
 7625. H
 7626. CH₃
 7627. CH₃
 1271. 7628. CH(CH₃)₂
 7629.


7630. CH₃
 7631. H
 7632. CH₃
 7633. CH₃
 1272. 7634. CH(CH₃)₂
 7635.


7636. CH₃
 7637. H
 7638. CH₃
 7639. CH₃
 1273. 7640. CH(CH₃)₂
 7641.


7642. CH₃
 7643. H
 7644. CH₃
 7645. CH₃
 1274. 7646. CH(CH₃)₂
 7647.


7648. CH₃
 7649. H
 7650. CH₃
 7651. CH₃
 1275. 7652. CH(CH₃)₂
 7653.


7654. CH₃
 7655. H
 7656. CH₃
 7657. CH₃
 1276. 7658. CH(CH₃)₂
 7659.


7660. CH₃
 7661. H
 7662. CH₃
 7663. CH₃
 1277. 7664. CH(CH₃)₂
 7665.


7666. CH₃
 7667. H
 7668. CH₃
 7669. CH₃
 1278. 7670. CD(CH₃)₂
 7671. CD₃
 7672. CD₃
 7673. H
 7674. CH₃
 7675. CH₃
 1279. 7676. CD(CH₃)₂
 7677. CD₂CD₃
 7678. CD₃
 7679. H
 7680. CH₃
 7681. CH₃
 1280. 7682. CD(CH₃)₂
 7683. CD₂CH₃
 7684. CD₃
 7685. H
 7686. CH₃
 7687. CH₃
 1281. 7688. CD(CH₃)₂
 7689. CD(CD₃)₂
 7690. CD₃
 7691. H
 7692. CH₃
 7693. CH₃
 1282. 7694. CD(CH₃)₂
 7695. CD(CH₃)₂
 7696. CD₃
 7697. H
 7698. CH₃
 7699. CH₃
 1283. 7700. CD(CH₃)₂
 7701. CD₂CD(CD₃)₂
 7702. CD₃
 7703. H
 7704. CH₃
 7705. CH₃
 1284. 7706. CD(CH₃)₂
 7707. CD₂CH(CH₃)₂
 7708. CD₃
 7709. H
 7710. CH₃
 7711. CH₃
 1285. 7712. CD(CH₃)₂
 7713. CD₂C(CD₃)₃
 7714. CD₃
 7715. H
 7716. CH₃
 7717. CH₃
 1286. 7718. CD(CH₃)₂
 7719. CD₂C(CH₃)₃
 7720. CD₃
 7721. H
 7722. CH₃
 7723. CH₃
 1287. 7724. CD(CH₃)₂
 7725. CD₂CD₂CF₃
 7726. CD₃
 7727. H
 7728. CH₃
 7729. CH₃
 1288. 7730. CD(CH₃)₂
 7731. CD₂CH₂CF₃
 7732. CD₃
 7733. H
 7734. CH₃
 7735. CH₃
 1289. 7736. CD(CH₃)₂
 7737. CD₂CCF₃(CH₃)₂
 7738. CD₃
 7739. H
 7740. CH₃
 7741. CH₃
 1290. 7742. CD(CH₃)₂
 7743.


7744. CD₃
 7745. H
 7746. CH₃
 7747. CH₃
 1291. 7748. CD(CH₃)₂
 7749.


7750. CD₃
 7751. H
 7752. CH₃
 7753. CH₃
 1292. 7754. CD(CH₃)₂
 7755.


7756. CD₃
 7757. H
 7758. CH₃
 7759. CH₃
 1293. 7760. CD(CH₃)₂
 7761.


7762. CD₃
 7763. H
 7764. CH₃
 7765. CH₃
 1294. 7766. CD(CH₃)₂
 7767.


7768. CD₃
 7769. H
 7770. CH₃
 7771. CH₃
 1295. 7772. CD(CH₃)₂
 7773.


7774. CD₃
 7775. H
 7776. CH₃
 7777. CH₃
 1296. 7778. CD(CH₃)₂
 7779.


7780. CD₃
 7781. H
 7782. CH₃
 7783. CH₃
 1297. 7784. CD(CH₃)₂
 7785.


7786. CD₃
 7787. H
 7788. CH₃
 7789. CH₃
 1298. 7790. CD(CH₃)₂
 7791.


7792. CD₃
 7793. H
 7794. CH₃
 7795. CH₃
 1299. 7796. CD(CH₃)₂
 7797.


7798. CD₃
 7799. H
 7800. CH₃
 7801. CH₃
 1300. 7802. CD(CH₃)₂
 7803.


7804. CD₃
 7805. H
 7806. CH₃
 7807. CH₃
 1301. 7808. CD(CH₃)₂
 7809.


7810. CD₃
 7811. H
 7812. CH₃
 7813. CH₃
 1302. 7814. CD(CH₃)₂
 7815.


7816. CD₃
 7817. H
 7818. CH₃
 7819. CH₃
 1303. 7820. CD(CH₃)₂
 7821.


7822. CD₃
 7823. H
 7824. CH₃
 7825. CH₃
 1304. 7826. CD(CH₃)₂
 7827.


7828. CD₃
 7829. H
 7830. CH₃
 7831. CH₃
 1305. 7832. CD(CH₃)₂
 7833.


7834. CD₃
 7835. H
 7836. CH₃
 7837. CH₃
 1306. 7838. CD(CH₃)₂
 7839.


7840. CD₃
 7841. H
 7842. CH₃
 7843. CH₃
 1307. 7844. CD(CH₃)₂
 7845.


7846. CD₃
 7847. H
 7848. CH₃
 7849. CH₃
 1308. 7850. CD(CH₃)₂
 7851.


7852. CD₃
 7853. H
 7854. CH₃
 7855. CH₃
 1309. 7856. CD(CH₃)₂
 7857.


7858. CD₃
 7859. H
 7860. CH₃
 7861. CH₃
 1310. 7862. CD(CD₃)₂
 7863. CD₂CD₃
 7864. CD₃
 7865. H
 7866. CD₂CD₃
 7867. CD₂CD₃
 1311. 7868. CD(CD₃)₂
 7869. CD₂CH₃
 7870. CD₃
 7871. H
 7872. CD₂CD₃
 7873. CD₂CD₃
 1312. 7874. CD(CD₃)₂
 7875. CD(CD₃)₂
 7876. CD₃
 7877. H
 7878. CD₂CD₃
 7879. CD₂CD₃
 1313. 7880. CD(CD₃)₂
 7881. CD(CH₃)₂
 7882. CD₃
 7883. H
 7884. CD₂CD₃
 7885. CD₂CD₃
 1314. 7886. CD(CD₃)₂
 7887. CD₂CD(CD₃)₂
 7888. CD₃
 7889. H
 7890. CD₂CD₃
 7891. CD₂CD₃
 1315. 7892. CD(CD₃)₂
 7893. CD₂CH(CH₃)₂
 7894. CD₃
 7895. H
 7896. CD₂CD₃
 7897. CD₂CD₃
 1316. 7898. CD(CD₃)₂
 7899. CD₂C(CD₃)₃
 7900. CD₃
 7901. H
 7902. CD₂CD₃
 7903. CD₂CD₃
 1317. 7904. CD(CD₃)₂
 7905. CD₂C(CH₃)₃
 7906. CD₃
 7907. H
 7908. CD₂CD₃
 7909. CD₂CD₃
 1318. 7910. CD(CD₃)₂
 7911. CD₂CD₂CF₃
 7912. CD₃
 7913. H
 7914. CD₂CD₃
 7915. CD₂CD₃
 1319. 7916. CD(CD₃)₂
 7917. CD₂CH₂CF₃
 7918. CD₃
 7919. H
 7920. CD₂CD₃
 7921. CD₂CD₃
 1320. 7922. CD(CD₃)₂
 7923. CD₂CCF₃(CH₃)₂
 7924. CD₃
 7925. H
 7926. CD₂CD₃
 7927. CD₂CD₃
 1321. 7928. CD(CD₃)₂
 7929.


7930. CD₃
 7931. H
 7932. CD₂CD₃
 7933. CD₂CD₃
 1322. 7934. CD(CD₃)₂
 7935.


7936. CD₃
 7937. H
 7938. CD₂CD₃
 7939. CD₂CD₃
 1323. 7940. CD(CD₃)₂
 7941.


7942. CD₃
 7943. H
 7944. CD₂CD₃
 7945. CD₂CD₃
 1324. 7946. CD(CD₃)₂
 7947.


7948. CD₃
 7949. H
 7950. CD₂CD₃
 7951. CD₂CD₃
 1325. 7952. CD(CD₃)₂
 7953.


7954. CD₃
 7955. H
 7956. CD₂CD₃
 7957. CD₂CD₃
 1326. 7958. CD(CD₃)₂
 7959.


7960. CD₃
 7961. H
 7962. CD₂CD₃
 7963. CD₂CD₃
 1327. 7964. CD(CD₃)₂
 7965.


7966. CD₃
 7967. H
 7968. CD₂CD₃
 7969. CD₂CD₃
 1328. 7970. CD(CD₃)₂
 7971.


7972. CD₃
 7973. H
 7974. CD₂CD₃
 7975. CD₂CD₃
 1329. 7976. CD(CD₃)₂
 7977.


7978. CD₃
 7979. H
 7980. CD₂CD₃
 7981. CD₂CD₃
 1330. 7982. CD(CD₃)₂
 7983.


7984. CD₃
 7985. H
 7986. CD₂CD₃
 7987. CD₂CD₃
 1331. 7988. CD(CD₃)₂
 7989.


7990. CD₃
 7991. H
 7992. CD₂CD₃
 7993. CD₂CD₃
 1332. 7994. CD(CD₃)₂
 7995.


7996. CD₃
 7997. H
 7998. CD₂CD₃
 7999. CD₂CD₃
 1333. 8000. CD(CD₃)₂
 8001.


8002. CD₃
 8003. H
 8004. CD₂CD₃
 8005. CD₂CD₃
 1334. 8006. CD(CD₃)₂
 8007.


8008. CD₃
 8009. H
 8010. CD₂CD₃
 8011. CD₂CD₃
 1335. 8012. CD(CD₃)₂
 8013.


8014. CD₃
 8015. H
 8016. CD₂CD₃
 8017. CD₂CD₃
 1336. 8018. CD(CD₃)₂
 8019.


8020. CD₃
 8021. H
 8022. CD₂CD₃
 8023. CD₂CD₃
 1337. 8024. CD(CD₃)₂
 8025.


8026. CD₃
 8027. H
 8028. CD₂CD₃
 8029. CD₂CD₃
 1338. 8030. CD(CD₃)₂
 8031.


8032. CD₃
 8033. H
 8034. CD₂CD₃
 8035. CD₂CD₃
 1339. 8036. CD(CD₃)₂
 8037.


8038. CD₃
 8039. H
 8040. CD₂CD₃
 8041. CD₂CD₃
 1340. 8042. CD(CD₃)₂
 8043.


8044. CD₃
 8045. H
 8046. CD₂CD₃
 8047. CD₂CD₃
 1341. 8048. CH(CH₃)₂
 8049. CH₃
 8050. CH₂CH₃
 8051. H
 8052. CD₂CD₃
 8053. CD₂CD₃
 1342. 8054. CH(CH₃)₂
 8055. CH₃
 8056. CH(CH₃)₂
 8057. H
 8058. CD₂CD₃
 8059. CD₂CD₃
 1343. 8060. CH(CH₃)₂
 8061. CH₃
 8062. CH₂CH(CH₃)₂
 8063. H
 8064. CD₂CD₃
 8065. CD₂CD₃
 1344. 8066. CH(CH₃)₂
 8067. CH₃
 8068. C(CH₃)₃
 8069. H
 8070. CD₂CD₃
 8071. CD₂CD₃
 1345. 8072. CH(CH₃)₂
 8073. CH₃
 8074. CH₂C(CH₃)₃
 8075. H
 8076. CD₂CD₃
 8077. CD₂CD₃
 1346. 8078. CH(CH₃)₂
 8079. CH₃
 8080. CH₂CH₂CF₃
 8081. H
 8082. CD₂CD₃
 8083. CD₂CD₃
 1347. 8084. CH(CH₃)₂
 8085. CH₃
 8086. CH₂CCF₃(CH₃)₂
 8087. H
 8088. CD₂CD₃
 8089. CD₂CD₃
 1348. 8090. CH(CH₃)₂
 8091. CH₃
 8092.


8093. H
 8094. CD₂CD₃
 8095. CD₂CD₃
 1349. 8096. CH(CH₃)₂
 8097. CH₃
 8098.


8099. H
 8100. CD₂CD₃
 8101. CD₂CD₃
 1350. 8102. CH(CH₃)₂
 8103. CH₃
 8104.


8105. H
 8106. CD₂CD₃
 8107. CD₂CD₃
 1351. 8108. CH(CH₃)₂
 8109. CH₃
 8110.


8111. H
 8112. CD₂CD₃
 8113. CD₂CD₃
 1352. 8114. CH(CH₃)₂
 8115. CH₃
 8116.


8117. H
 8118. CD₂CD₃
 8119. CD₂CD₃
 1353. 8120. CH(CH₃)₂
 8121. CH₃ 8122 .


8123. H
 8124. CD₂CD₃
 8125. CD₂CD₃
 1354. 8126. CH(CH₃)₂
 8127. CH₃
 8128.


8129. H
 8130. CD₂CD₃
 8131. CD₂CD₃
 1355. 8132. CH(CH₃)₂
 8133. CH₃
 8134.


8135. H
 8136. CD₂CD₃
 8137. CD₂CD₃
 1356. 8138. CH(CH₃)₂
 8139. CH₃
 8140.


8141. H
 8142. CD₂CD₃
 8143. CD₂CD₃
 1357. 8144. CH(CH₃)₂
 8145. CH₃
 8146.


8147. H
 8148. CD₂CD₃
 8149. CD₂CD₃
 1358. 8150. CH(CH₃)₂
 8151. CH₃
 8152.


8153. H
 8154. CD₂CD₃
 8155. CD₂CD₃
 1359. 8156. CH(CH₃)₂
 8157. CH₃
 8158.


8159. H
 8160. CD₂CD₃
 8161. CD₂CD₃
 1360. 8162. CH(CH₃)₂
 8163. CH₃
 8164.


8165. H
 8166. CD₂CD₃
 8167. CD₂CD₃
 1361. 8168. CH(CH₃)₂
 8169. CH₃
 8170.


8171. H
 8172. CD₂CD₃
 8173. CD₂CD₃
 1362. 8174. CH(CH₃)₂
 8175. CH₃
 8176.


8177. H
 8178. CD₂CD₃
 8179. CD₂CD₃
 1363. 8180. CH(CH₃)₂
 8181. CH₃
 8182.


8183. H
 8184. CD₂CD₃
 8185. CD₂CD₃
 1364. 8186. CH(CH₃)₂
 8187. CH₃
 8188.


8189. H
 8190. CD₂CD₃
 8191. CD₂CD₃
 1365. 8192. CH(CH₃)₂
 8193. CH₃
 8194.


8195. H
 8196. CD₂CD₃
 8197. CD₂CD₃
 1366. 8198. CH(CH₃)₂
 8199. CH₃
 8200.


8201. H
 8202. CD₂CD₃
 8203. CD₂CD₃
 1367. 8204. CH(CH₃)₂
 8205. CH₃
 8206.


8207. H
 8208. CD₂CD₃
 8209. CD₂CD₃
 1368. 8210. CD(CH₃)₂
 8211. CD₃
 8212. CD₂CD₃
 8213. H
 8214. CD₂CD₃
 8215. CD₂CD₃
 1369. 8216. CD(CH₃)₂
 8217. CD₃
 8218. CD₂CH₃
 8219. H
 8220. CD₂CD₃
 8221. CD₂CD₃
 1370. 8222. CD(CH₃)₂
 8223. CD₃
 8224. CD(CD₃)₂
 8225. H
 8226. CD₂CD₃
 8227. CD₂CD₃
 1371. 8228. CD(CH₃)₂
 8229. CD₃
 8230. CD(CH₃)₂
 8231. H
 8232. CD₂CD₃
 8233. CD₂CD₃
 1372. 8234. CD(CH₃)₂
 8235. CD₃
 8236. CD₂CD(CD₃)₂
 8237. H
 8238. CD₂CD₃
 8239. CD₂CD₃
 1373. 8240. CD(CH₃)₂
 8241. CD₃
 8242. CD₂CH(CH₃)₂
 8243. H
 8244. CD₂CD₃
 8245. CD₂CD₃
 1374. 8246. CD(CH₃)₂
 8247. CD₃
 8248. CD₂C(CD₃)₃
 8249. H
 8250. CD₂CD₃
 8251. CD₂CD₃
 1375. 8252. CD(CH₃)₂
 8253. CD₃
 8254. CD₂C(CH₃)₃
 8255. H
 8256. CD₂CD₃
 8257. CD₂CD₃
 1376. 8258. CD(CH₃)₂
 8259. CD₃
 8260. CD₂CD₂CF₃
 8261. H
 8262. CD₂CD₃
 8263. CD₂CD₃
 1377. 8264. CD(CH₃)₂
 8265. CD₃
 8266. CD₂CH₂CF₃
 8267. H
 8268. CD₂CD₃
 8269. CD₂CD₃
 1378. 8270. CD(CH₃)₂
 8271. CD₃
 8272. CD₂CCF₃(CH₃)₂
 8273. H
 8274. CD₂CD₃
 8275. CD₂CD₃
 1379. 8276. CD(CH₃)₂
 8277. CD₃
 8278.


8279. H
 8280. CD₂CD₃
 8281. CD₂CD₃
 1380. 8282. CD(CH₃)₂
 8283. CD₃
 8284.


8285. H
 8286. CD₂CD₃
 8287. CD₂CD₃
 1381. 8288. CD(CH₃)₂
 8289. CD₃
 8290.


8291. H
 8292. CD₂CD₃
 8293. CD₂CD₃
 1382. 8294. CD(CH₃)₂
 8295. CD₃
 8296.


8297. H
 8298. CD₂CD₃
 8299. CD₂CD₃
 1383. 8300. CD(CH₃)₂
 8301. CD₃
 8302.


8303. H
 8304. CD₂CD₃
 8305. CD₂CD₃
 1384. 8306. CD(CH₃)₂
 8307. CD₃
 8308.


8309. H
 8310. CD₂CD₃
 8311. CD₂CD₃
 1385. 8312. CD(CH₃)₂
 8313. CD₃
 8314.


8315. H
 8316. CD₂CD₃
 8317. CD₂CD₃
 1386. 8318. CD(CH₃)₂
 8319. CD₃
 8320.


8321. H
 8322. CD₂CD₃
 8323. CD₂CD₃
 1387. 8324. CD(CH₃)₂
 8325. CD₃
 8326.


8327. H
 8328. CD₂CD₃
 8329. CD₂CD₃
 1388. 8330. CD(CH₃)₂
 8331. CD₃
 8332.


8333. H
 8334. CD₂CD₃
 8335. CD₂CD₃
 1389. 8336. CD(CH₃)₂
 8337. CD₃
 8338.


8339. H
 8340. CD₂CD₃
 8341. CD₂CD₃
 1390. 8342. CD(CH₃)₂
 8343. CD₃
 8344.


8345. H
 8346. CD₂CD₃
 8347. CD₂CD₃
 1391. 8348. CD(CH₃)₂
 8349. CD₃
 8350.


8351. H
 8352. CD₂CD₃
 8353. CD₂CD₃
 1392. 8354. CD(CH₃)₂
 8355. CD₃
 8356.


8357. H
 8358. CD₂CD₃
 8359. CD₂CD₃
 1393. 8360. CD(CH₃)₂
 8361. CD₃
 8362.


8363. H
 8364. CD₂CD₃
 8365. CD₂CD₃
 1394. 8366. CD(CH₃)₂
 8367. CD₃
 8368.


8369. H
 8370. CD₂CD₃
 8371. CD₂CD₃
 1395. 8372. CD(CH₃)₂
 8373. CD₃
 8374.


8375. H
 8376. CD₂CD₃
 8377. CD₂CD₃
 1396. 8378. CD(CH₃)₂
 8379. CD₃
 8380.


8381. H
 8382. CD₂CD₃
 8383. CD₂CD₃
 1397. 8384. CD(CH₃)₂
 8385. CD₃
 8386.


8387. H
 8388. CD₂CD₃
 8389. CD₂CD₃
 1398. 8390. CD(CH₃)₂
 8391. CD₃
 8392.


8393. H
 8394. CD₂CD₃
 8395. CD₂CD₃
 1399. 8396.


8397. CD₃
 8398. H
 8399. H
 8400. H
 8401. CD₃
 1400. 8402.


8403. CD₃
 8404. CD₃
 8405. H
 8406. H
 8407. CD₃
 1401. 8408.


8409. CD₃
 8410. H
 8411. CD₃
 8412. H
 8413. CD₃
 1402. 8414.


8415. CD₃
 8416. CD₃
 8417. CD₃
 8418. H
 8419. CD₃
 1403. 8420.


8421. CD₃
 8422. H
 8423. H
 8424. H
 8425. CD₃
 1404. 8426.


8427. CD₃
 8428. CD₃
 8429. H
 8430. H
 8431. CD₃
 1405. 8432.


8433. CD₃
 8434. H
 8435. CD₃
 8436. H
 8437. CD₃
 1406. 8438.


8439. CD₃
 8440. CD₃
 8441. CD₃
 8442. H
 8443. CD₃
 1407. 8444.


8445. CD₃
 8446. H
 8447. H
 8448. H
 8449. CD₃
 1408. 8450.


8451. CD₃
 8452. CD₃
 8453. H
 8454. H
 8455. CD₃
 1409. 8456.


8457. CD₃
 8458. H
 8459. CD₃
 8460. H
 8461. CD₃
 1410. 8462.


8463. CD₃
 8464. CD₃
 8465. CD₃
 8466. H
 8467. CD₃
 1411. 8468.


8469. CD₃
 8470. H
 8471. H
 8472. H
 8473. CD₃
 1412. 8474.


8475. CD₃
 8476. CD₃
 8477. H
 8478. H
 8479. CD₃
 1413. 8480.


8481. CD₃
 8482. H
 8483. CD₃
 8484. H
 8485. CD₃
 1414. 8486.


8487. CD₃
 8488. CD₃
 8489. CD₃
 8490. H
 8491. CD₃
 1415. 8492.


8493. CD₃
 8494. H
 8495. H
 8496. H
 8497. CD₃
 1416. 8498.


8499. CD₃
 8500. CD₃
 8501. H
 8502. H
 8503. CD₃
 1417. 8504.


8505. CD₃
 8506. H
 8507. CD₃
 8508. H
 8509. CD₃
 1418. 8510.


8511. CD₃
 8512. CD₃
 8513. CD₃
 8514. H
 8515. CD₃
 1419. 8516.


8517. CD₃
 8518. H
 8519. H
 8520. H
 8521. CD₃
 1420. 8522.


8523. CD₃
 8524. CD₃
 8525. H
 8526. H
 8527. CD₃
 1421. 8528.


8529. CD₃
 8530. H
 8531. CD₃
 8532. H
 8533. CD₃
 1422. 8534.


8535. CD₃
 8536. CD₃
 8537. CD₃
 8538. H
 8539. CD₃
 1423. 8540.


8541. CD₃
 8542. H
 8543. H
 8544. H
 8545. CD₃
 1424. 8546.


8547. CD₃
 8548. CD₃
 8549. H
 8550. H
 8551. CD₃
 1425. 8552.


8553. CD₃
 8554. H
 8555. CD₃
 8556. H
 8557. CD₃
 1426. 8558.


8559. CD₃
 8560. CD₃
 8561. CD₃
 8562. H
 8563. CD₃
 1427. 8564.


8565. CD₃
 8566. H
 8567. H
 8568. H
 8569. CD₃
 1428. 8570.


8571. CD₃
 8572. CD₃
 8573. H
 8574. H
 8575. CD₃
 1429. 8576.


8577. CD₃
 8578. H
 8579. CD₃
 8580. H
 8581. H
 1430. 8582.


8583. CD₃
 8584. CD₃
 8585. CD₃
 8586. H
 8587. H
 1431. 8588. D₃
 8589. H
 8590. H
 8591.


8592. H
 8593. H
 1432. 8594. D₃
 8595. CD₃
 8596. CD₃
 8597. H
 8598. H
 8599. H


13. The compound of claim 1, wherein the compound has a formula of ML_(n)(L_(B))_(m-n); wherein M is Ir or Pt; wherein L_(B) is a bidentate ligand; wherein, when M is Ir, m is 3, and n is 1, 2, or 3; and wherein, when M is Pt, m is 2, and n is 1, or
 2. 14. The compound of claim 13, wherein the compound has a formula of IrL₃, IrL(L_(B))₂, or Ir(L)₂(L_(B)), wherein L_(B) is different from L; or the compound has a formula of or Pt(L)(L_(B)), wherein L and L_(B) can be the same or different. 15.-19. (canceled)
 20. The compound of claim 13, wherein, when M is Ir, m is 3, and n is 1 or 2; wherein, when M is Pt, m is 2, and n is 1; and wherein L_(B) is selected from the group consisting of:

wherein each X¹ to X¹³ are independently selected from the group consisting of carbon and nitrogen; wherein X is selected from the group consisting of BR′, NR′, PR′, O, S, Se, C═O, S═O, SO₂, CR′R″, SiR′R″, and GeR′R″; wherein R′ and R″ are optionally fused or joined to form a ring; wherein each R_(a), R_(b), R_(c), and R_(d) may represent from mono substitution to the possible maximum number of substitution, or no substitution; wherein R′, R″, R_(a), R_(b), R_(c), and R_(d) are each independently selected from the group consisting of hydrogen, deuterium, halide, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acids, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof; and wherein any two adjacent substitutents of R_(a), R_(b), R_(c), and R_(d) are optionally fused or joined to form a ring or form a multidentate ligand.
 21. The compound of claim 13, wherein, when M is Ir, m is 3, and n is 1 or 2; wherein, when M is Pt, m is 2, and n is 1; and wherein L_(B) is selected from the group consisting of L_(B1) to L_(B300) as shown below:


22. The compound of claim 12, wherein the compound is selected from the group consisting of compound A-1 to compound A-429,600, compound B-1 to compound B-429,600, compound C-1 to compound C-429,600, and compound D-1 to compound D-429,600; wherein Compound k-x has the formula Ir(L^(ki))(L_(Bj))₂; wherein x=300i+j−300; k is A, B, C, or D; i is an integer from 1 to 1432, and j is an integer from 1 to 300; wherein L_(B1) to L_(B300) have the following structure:


23. The compound of claim 1, wherein the compound is incorporated into a chemical formula.
 24. An organic light emitting device (OLED) comprising: an anode; a cathode; and an organic layer, disposed between the anode and the cathode, comprising a compound comprising a ligand L having the formula:

wherein R¹ and R⁶ represents mono, di, tri, or tetra substitution, or no substitution; wherein R² represents mono, di, or tri substitution, or no substitution; wherein each R¹, R², R³, R⁴, R⁴, R⁵, R⁶, R⁷, and R⁸ is independently selected from the group consisting of hydrogen, deuterium, halide, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acids, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof; wherein any adjacent substituents of R¹ R², R³, R⁴, R⁵, R⁶, R⁷, and R⁸ are optionally joined or fused into a ring; wherein at least one of R³, R⁴, and R⁵ is not hydrogen; wherein a is an integer from 0 to 10; wherein (i) when a is 0, at least one of R⁷, R⁸, and an R² adjacent to ring B, is not hydrogen, and (ii) when a is 1 to 10, at least one of an R² adjacent to ring A and an R⁶ adjacent to ring C is not hydrogen; wherein the ligand L is coordinated to a metal M having an atomic weight greater than 40; and wherein the ligand L is optionally linked with other ligands to comprise a tridentate, tetradentate, pentadentate or hexadentate ligand.
 25. The OLED of claim 24, wherein the organic layer is an emissive layer and the compound is an emissive dopant or a non-emissive dopant.
 26. (canceled)
 27. The OLED of claim 24, wherein the organic layer further comprises a host, wherein host comprises at least one chemical group selected from the group consisting of triphenylene, carbazole, dibenzothiphene, dibenzofuran, dibenzoselenophene, azatriphenylene, azacarbazole, aza-dibenzothiophene, aza-dibenzofuran, and aza-dibenzoselenophene.
 28. The OLED of claim 24, wherein the organic layer further comprises a host, wherein the host is selected from the group consisting of:

and combinations thereof.
 29. (canceled)
 30. A consumer product comprising an organic light-emitting device comprising: an anode; a cathode; and an organic layer, disposed between the anode and the cathode, comprising a compound comprising a ligand L having the formula:

wherein R¹ and R⁶ represents mono, di, tri, or tetra substitution, or no substitution; wherein R² represents mono, di, or tri substitution, or no substitution; wherein each R¹, R², R³, R⁴, R⁴, R⁵, R⁶, R⁷, and R⁸ is independently selected from the group consisting of hydrogen, deuterium, halide, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acids, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof; wherein any adjacent substituents of R¹ R², R³, R⁴, R⁵, R⁶, R⁷, and R⁸ are optionally joined or fused into a ring; wherein at least one of R³, R⁴, and R⁵ is not hydrogen; wherein a is an integer from 0 to 10; wherein (i) when a is 0, at least one of R⁷, R⁸, and an R² adjacent to ring B, is not hydrogen, and (ii) when a is 1 to 10, at least one of an R² adjacent to ring A and an R⁶ adjacent to ring C is not hydrogen; wherein the ligand L is coordinated to a metal M having an atomic weight greater than 40; and wherein the ligand L is optionally linked with other ligands to comprise a tridentate, tetradentate, pentadentate or hexadentate ligand.
 31. The consumer product in claim 30, wherein the consumer product is selected from the group consisting of flat panel displays, computer monitors, medical monitors, televisions, billboards, lights for interior or exterior illumination and/or signaling, heads-up displays, fully or partially transparent displays, flexible displays, laser printers, telephones, cell phones, tablets, phablets, personal digital assistants (PDAs), wearable device, laptop computers, digital cameras, camcorders, viewfinders, micro-displays, 3-D displays, virtual reality or augmented reality displays, vehicles, a large area wall, theater or stadium screen, and a sign. 